Technology dictates algorithms: recent developments in read alignment
暂无分享,去创建一个
C. Alkan | O. Mutlu | M. Alser | B. Balliu | A. Zelikovsky | D. Koslicki | Huwenbo Shi | S. Mangul | Jeremy Rotman | B. Singer | Dhrithi Deshpande | H. Yang | P. Skums | P. Baykal | S. Knyazev | K. Taraszka | Victor Xue
[1] Richard W. Hamming,et al. Error detecting and error correcting codes , 1950 .
[2] S. B. Needleman,et al. A general method applicable to the search for similarities in the amino acid sequence of two proteins. , 1970, Journal of molecular biology.
[3] M S Waterman,et al. Identification of common molecular subsequences. , 1981, Journal of molecular biology.
[4] D. Lipman,et al. Rapid similarity searches of nucleic acid and protein data banks. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[5] Esko Ukkonen,et al. Algorithms for Approximate String Matching , 1985, Inf. Control..
[6] Richard M. Karp,et al. Efficient Randomized Pattern-Matching Algorithms , 1987, IBM J. Res. Dev..
[7] D. Lipman,et al. Improved tools for biological sequence comparison. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[8] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[9] Esko Ukkonen,et al. Approximate String-Matching over Suffix Trees , 1993, CPM.
[10] Uzi Vishkin,et al. Efficient approximate and dynamic matching of patterns using a labeling paradigm , 1996, Proceedings of 37th Conference on Foundations of Computer Science.
[11] Thomas L. Madden,et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. , 1997, Nucleic acids research.
[12] Richard Cole,et al. Approximate string matching: a simpler faster algorithm , 2002, SODA '98.
[13] J. Mullikin,et al. SSAHA: a fast search method for large DNA databases. , 2001, Genome research.
[14] W. J. Kent,et al. BLAT--the BLAST-like alignment tool. , 2002, Genome research.
[15] Bin Ma,et al. PatternHunter: faster and more sensitive homology search , 2002, Bioinform..
[16] Cristian S. Calude,et al. Additive Distances and Quasi-Distances Between Words , 2002, J. Univers. Comput. Sci..
[17] J. Weissenbach. Human genome project: past, present, future. , 2002, Ernst Schering Research Foundation workshop.
[18] S. Salzberg,et al. Fast algorithms for large-scale genome alignment and comparison. , 2002, Nucleic acids research.
[19] Juha Kärkkäinen,et al. Better Filtering with Gapped q-Grams , 2001, Fundam. Informaticae.
[20] Inna Dubchak,et al. Glocal alignment: finding rearrangements during alignment , 2003, ISMB.
[21] D. Haussler,et al. Human-mouse alignments with BLASTZ. , 2003, Genome research.
[22] S. Salzberg,et al. Versatile and open software for comparing large genomes , 2004, Genome Biology.
[23] Daniel Shawcross Wilkerson,et al. Winnowing: local algorithms for document fingerprinting , 2003, SIGMOD '03.
[24] Michael Roberts,et al. Reducing storage requirements for biological sequence comparison , 2004, Bioinform..
[25] Ewan Birney,et al. Automated generation of heuristics for biological sequence comparison , 2005, BMC Bioinformatics.
[26] Robert C. Edgar,et al. MUSCLE: multiple sequence alignment with high accuracy and high throughput. , 2004, Nucleic acids research.
[27] Sean R Eddy,et al. What is dynamic programming? , 2004, Nature Biotechnology.
[28] Thomas D. Wu,et al. GMAP: a genomic mapping and alignment program for mRNA and EST sequence , 2005, Bioinform..
[29] Thomas Lengauer,et al. Data and text mining Computational methods for the design of effective therapies against drug resistant HIV strains , 2005 .
[30] Philip Hugenholtz,et al. NAST: a multiple sequence alignment server for comparative analysis of 16S rRNA genes , 2006, Nucleic Acids Res..
[31] Michael Q. Zhang,et al. Using quality scores and longer reads improves accuracy of Solexa read mapping , 2008, BMC Bioinformatics.
[32] M. Schatz,et al. Genome assembly forensics: finding the elusive mis-assembly , 2008, Genome Biology.
[33] Alexander F. Auch,et al. MEGAN analysis of metagenomic data. , 2007, Genome research.
[34] S. Nelson,et al. Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning , 2008, Nature.
[35] Joshua M. Korn,et al. Association between microdeletion and microduplication at 16p11.2 and autism. , 2008, The New England journal of medicine.
[36] Brian D. Ondov,et al. Efficient mapping of Applied Biosystems SOLiD sequence data to a reference genome for functional genomic applications , 2008, Bioinform..
[37] Gunnar Rätsch,et al. Optimal spliced alignments of short sequence reads , 2008, BMC Bioinformatics.
[38] Wing Hung Wong,et al. SeqMap: mapping massive amount of oligonucleotides to the genome , 2008, Bioinform..
[39] Gunnar Rätsch,et al. Optimal spliced alignments of short sequence reads , 2008, ECCB.
[40] Hanlee P. Ji,et al. Next-generation DNA sequencing , 2008, Nature Biotechnology.
[41] Ruiqiang Li,et al. SOAP: short oligonucleotide alignment program , 2008, Bioinform..
[42] Siu-Ming Yiu,et al. Compressed indexing and local alignment of DNA , 2008, Bioinform..
[43] Joshua M. Korn,et al. Mapping and sequencing of structural variation from eight human genomes , 2008, Nature.
[44]
R. Durbin,et al.
Mapping Quality Scores Mapping Short Dna Sequencing Reads and Calling Variants Using P ,
2022
.
[45]
Bin Ma,et al.
ZOOM! Zillions of oligos mapped
,
2008,
Bioinform..
[46]
Cole Trapnell,et al.
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
,
2009,
Genome Biology.
[47]
S. Nelson,et al.
BFAST: An Alignment Tool for Large Scale Genome Resequencing
,
2009,
PloS one.
[48]
Paul Flicek,et al.
Sense from sequence reads: methods for alignment and assembly
,
2009,
Nature Methods.
[49]
Mihai Pop,et al.
Inexact Local Alignment Search over Suffix Arrays
,
2009,
2009 IEEE International Conference on Bioinformatics and Biomedicine.
[50]
N. Warthmann,et al.
Simultaneous alignment of short reads against multiple genomes
,
2009,
Genome Biology.
[51]
Michael C. Schatz,et al.
CloudBurst: highly sensitive read mapping with MapReduce
,
2009,
Bioinform..
[52]
Peter F. Stadler,et al.
Fast Mapping of Short Sequences with Mismatches, Insertions and Deletions Using Index Structures
,
2009,
PLoS Comput. Biol..
[53]
Wei Li,et al.
BSMAP: whole genome bisulfite sequence MAPping program
,
2009,
BMC Bioinformatics.
[54]
J. Kitzman,et al.
Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing
,
2009,
Nature Genetics.
[55]
Lior Pachter,et al.
Sequence Analysis
,
2020,
Definitions.
[56]
Yuan Gao,et al.
MOM: maximum oligonucleotide mapping
,
2009,
Bioinform..
[57]
Michael Brudno,et al.
SHRiMP: Accurate Mapping of Short Color-space Reads
,
2009,
PLoS Comput. Biol..
[58]
K. Reinert,et al.
RazerS--fast read mapping with sensitivity control.
,
2009,
Genome research.
[59]
Martin Hartmann,et al.
Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities
,
2009,
Applied and Environmental Microbiology.
[60]
Steven J. M. Jones,et al.
Slider—maximum use of probability information for alignment of short sequence reads and SNP detection
,
2008,
Bioinform..
[61]
Richard Durbin,et al.
Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform
,
2009
.
[62]
Giorgio Valle,et al.
PASS: a program to align short sequences
,
2009,
Bioinform..
[63]
Siu-Ming Yiu,et al.
SOAP2: an improved ultrafast tool for short read alignment
,
2009,
Bioinform..
[64]
Pao-Yang Chen,et al.
BS Seeker: precise mapping for bisulfite sequencing
,
2010,
BMC Bioinformatics.
[65]
Ting Chen,et al.
PerM: efficient mapping of short sequencing reads with periodic full sensitive spaced seeds
,
2009,
Bioinform..
[66]
Steven J. M. Jones,et al.
High quality SNP calling using Illumina data at shallow coverage
,
2010,
Bioinform..
[67]
B. Langmead,et al.
Aligning Short Sequencing Reads with Bowtie
,
2010,
Current protocols in bioinformatics.
[68]
Michael Q. Zhang,et al.
Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications
,
2010,
Nature Biotechnology.
[69]
Knut Reinert,et al.
MicroRazerS: rapid alignment of small RNA reads
,
2010,
Bioinform..
[70]
Ion I. Mandoiu,et al.
Estimation of alternative splicing isoform frequencies from RNA-Seq data
,
2010,
Algorithms for Molecular Biology.
[71]
Zemin Ning,et al.
SMALT – A new mapper for DNA sequencing reads
,
2010
.
[72]
Rob Knight,et al.
PyNAST: a flexible tool for aligning sequences to a template alignment
,
2009,
Bioinform..
[73]
Dominique Lavenier,et al.
GASSST: global alignment short sequence search tool
,
2010,
Bioinform..
[74]
Vipin T. Sreedharan,et al.
RNA‐Seq Read Alignments with PALMapper
,
2010,
Current protocols in bioinformatics.
[75]
Mark J. Clement,et al.
The GNUMAP algorithm: unbiased probabilistic mapping of oligonucleotides from next-generation sequencing
,
2010,
Bioinform..
[76]
M. Metzker.
Sequencing technologies — the next generation
,
2010,
Nature Reviews Genetics.
[77]
Faraz Hach,et al.
mrsFAST: a cache-oblivious algorithm for short-read mapping
,
2010,
Nature Methods.
[78]
Weng-Keen Wong,et al.
Gene expression Advance Access publication April 21, 2010 Supersplat—spliced RNA-seq alignment
,
2009
.
[79]
Serban Nacu,et al.
Fast and SNP-tolerant detection of complex variants and splicing in short reads
,
2010,
Bioinform..
[80]
Richard Durbin,et al.
Fast and accurate long-read alignment with Burrows–Wheeler transform
,
2010,
Bioinform..
[81]
Y. Xing,et al.
Detection of splice junctions from paired-end RNA-seq data by SpliceMap
,
2010,
Nucleic acids research.
[82]
Derek Y. Chiang,et al.
MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery
,
2010,
Nucleic acids research.
[83]
R. Sanjuán,et al.
Viral Mutation Rates
,
2010,
Journal of Virology.
[84]
Heng Li,et al.
A survey of sequence alignment algorithms for next-generation sequencing
,
2010,
Briefings Bioinform..
[85]
Martin Kircher,et al.
Addressing challenges in the production and analysis of illumina sequencing data
,
2011,
BMC Genomics.
[86]
M. Frith,et al.
Adaptive seeds tame genomic sequence comparison.
,
2011,
Genome research.
[87]
Lucian Ilie,et al.
SHRiMP2: Sensitive yet Practical Short Read Mapping
,
2011,
Bioinform..
[88]
Jignesh M. Patel,et al.
WHAM: A High-Throughput Sequence Alignment Method
,
2011,
TODS.
[89]
Sean M. Grimmond,et al.
X-MATE: a flexible system for mapping short read data
,
2011,
Bioinform..
[90]
Costas S. Iliopoulos,et al.
DynMap: mapping short reads to multiple related genomes
,
2011,
BCB '11.
[91]
Siu-Ming Yiu,et al.
SOAPsplice: Genome-Wide ab initio Detection of Splice Junctions from RNA-Seq Data
,
2011,
Front. Gene..
[92]
Rob Knight,et al.
Using QIIME to Analyze 16S rRNA Gene Sequences from Microbial Communities
,
2011,
Current protocols in bioinformatics.
[93]
Nicholas Eriksson,et al.
ShoRAH: estimating the genetic diversity of a mixed sample from next-generation sequencing data
,
2011,
BMC Bioinformatics.
[94]
Stefan R. Henz,et al.
Reference-guided assembly of four diverse Arabidopsis thaliana genomes
,
2011,
Proceedings of the National Academy of Sciences.
[95]
Felix Krueger,et al.
Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications
,
2011,
Bioinform..
[96]
Martin Goodson,et al.
Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads.
,
2011,
Genome research.
[97]
Ümit V. Çatalyürek,et al.
Benchmarking short sequence mapping tools
,
2013,
BMC Bioinformatics.
[98]
Richard M. Karp,et al.
Faster and More Accurate Sequence Alignment with SNAP
,
2011,
ArXiv.
[99]
Wei-keng Liao,et al.
Anatomy of a hash-based long read sequence mapping algorithm for next generation DNA sequencing
,
2011,
Bioinform..
[100]
Wing-Kin Sung,et al.
BatMis: a fast algorithm for k-mismatch mapping
,
2012,
Bioinform..
[101]
Wing Hung Wong,et al.
Fast and accurate read alignment for resequencing
,
2012,
Bioinform..
[102]
Jiang Li,et al.
The effect of strand bias in Illumina short-read sequencing data
,
2012,
BMC Genomics.
[103]
Elizabeth M. Ryan,et al.
De novo assembly of highly diverse viral populations
,
2012,
BMC Genomics.
[104]
Véronique Martin,et al.
Mapping Reads on a Genomic Sequence: An Algorithmic Overview and a Practical Comparative Analysis
,
2012,
J. Comput. Biol..
[105]
Nuno A. Fonseca,et al.
Tools for mapping high-throughput sequencing data
,
2012,
Bioinform..
[106]
Stefano Lonardi,et al.
BRAT-BW: efficient and accurate mapping of bisulfite-treated reads
,
2012,
Bioinform..
[107]
Ira M. Hall,et al.
YAHA: fast and flexible long-read alignment with optimal breakpoint detection
,
2012,
Bioinform..
[108]
Peter H. Sudmant,et al.
Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication
,
2012,
Cell.
[109]
Cole Trapnell,et al.
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
,
2013,
Genome Biology.
[110]
E. Domingo,et al.
Viral Quasispecies Evolution
,
2012,
Microbiology and Molecular Reviews.
[111]
Steven L Salzberg,et al.
Fast gapped-read alignment with Bowtie 2
,
2012,
Nature Methods.
[112]
Roderic Guigó,et al.
The GEM mapper: fast, accurate and versatile alignment by filtration
,
2012,
Nature Methods.
[113]
Yongchao Liu,et al.
Long read alignment based on maximal exact match seeds
,
2012,
Bioinform..
[114]
C. Huttenhower,et al.
Metagenomic microbial community profiling using unique clade-specific marker genes
,
2012,
Nature Methods.
[115]
Pavel Skums,et al.
Efficient error correction for next-generation sequencing of viral amplicons
,
2012,
BMC Bioinformatics.
[116]
Yongan Zhao,et al.
RAPSearch2: a fast and memory-efficient protein similarity search tool for next-generation sequencing data
,
2011,
Bioinform..
[117]
Eric Rivals,et al.
CRAC: an integrated approach to the analysis of RNA-seq reads
,
2013,
Genome Biology.
[118]
Nagesh V. Honnalli,et al.
Hobbes: optimized gram-based methods for efficient read alignment
,
2011,
Nucleic acids research.
[119]
Jun Hu,et al.
OSA: a fast and accurate alignment tool for RNA-Seq
,
2012,
Bioinform..
[120]
Martin Vingron,et al.
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS
,
2012,
Bioinform..
[121]
Knut Reinert,et al.
RazerS 3: Faster, fully sensitive read mapping
,
2012,
Bioinform..
[122]
Kai Ye,et al.
PASSion: a pattern growth algorithm-based pipeline for splice junction detection in paired-end RNA-Seq data
,
2012,
Bioinform..
[123]
Glenn Tesler,et al.
Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory
,
2012,
BMC Bioinformatics.
[124]
Chung F. Wong,et al.
SRmapper: a fast and sensitive genome-hashing alignment tool
,
2013,
Bioinform..
[125]
W. Shi,et al.
The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote
,
2013,
Nucleic acids research.
[126]
J. Harrow,et al.
Systematic evaluation of spliced alignment programs for RNA-seq data
,
2013,
Nature Methods.
[127]
Michael Q. Zhang,et al.
BS-Seeker2: a versatile aligning pipeline for bisulfite sequencing data
,
2013,
BMC Genomics.
[128]
Arndt von Haeseler,et al.
NextGenMap: fast and accurate read mapping in highly polymorphic genomes
,
2013,
Bioinform..
[129]
Sean R. Eddy,et al.
Infernal 1.1: 100-fold faster RNA homology searches
,
2013,
Bioinform..
[130]
Onur Mutlu,et al.
Accelerating read mapping with FastHASH
,
2013,
BMC Genomics.
[131]
Giovanni Manzini,et al.
Better spaced seeds using Quadratic Residues
,
2013,
J. Comput. Syst. Sci..
[132]
Xiaohui Xie,et al.
Improving read mapping using additional prefix grams
,
2014,
BMC Bioinformatics.
[133]
Heng Li.
Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
,
2013,
1303.3997.
[134]
Thomas R. Gingeras,et al.
STAR: ultrafast universal RNA-seq aligner
,
2013,
Bioinform..
[135]
Derrick E. Wood,et al.
Kraken: ultrafast metagenomic sequence classification using exact alignments
,
2014,
Genome Biology.
[136]
Sahar Al Seesi,et al.
Transcriptome assembly and quantification from Ion Torrent RNA-Seq data
,
2013,
BMC Genomics.
[137]
Volker Roth,et al.
Probabilistic Inference of Viral Quasispecies Subject to Recombination
,
2013,
J. Comput. Biol..
[138]
M. Pop,et al.
Sequence assembly demystified
,
2013,
Nature Reviews Genetics.
[139]
Ion I. Mandoiu,et al.
Reconstruction of viral population structure from next-generation sequencing data using multicommodity flows
,
2013,
BMC Bioinformatics.
[140]
Xiao Yang,et al.
V-Phaser 2: variant inference for viral populations
,
2013,
BMC Genomics.
[141]
M. Berriman,et al.
REAPR: a universal tool for genome assembly evaluation
,
2013,
Genome Biology.
[142]
Knut Reinert,et al.
Fast and accurate read mapping with approximate seeds and multiple backtracking
,
2012,
Nucleic acids research.
[143]
Inanç Birol,et al.
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species
,
2013,
GigaScience.
[144]
Aaron A. Klammer,et al.
Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data
,
2013,
Nature Methods.
[145]
Anqi Wang,et al.
SEME: A Fast Mapper of Illumina Sequencing Reads with Statistical Evaluation
,
2013,
RECOMB.
[146]
Steven J. M. Jones,et al.
JAGuaR: Junction Alignments to Genome for RNA-Seq Reads
,
2014,
PloS one.
[147]
Yongchao Liu,et al.
CUSHAW3: Sensitive and Accurate Base-Space and Color-Space Short-Read Alignment with Hybrid Seeding
,
2014,
PloS one.
[148]
Anders Krogh,et al.
Adaptable probabilistic mapping of short reads using position specific scoring matrices
,
2014,
BMC Bioinformatics.
[149]
Faraz Hach,et al.
mrsFAST-Ultra: a compact, SNP-aware mapper for high performance sequencing applications
,
2014,
Nucleic Acids Res..
[150]
Volker Roth,et al.
HIV Haplotype Inference Using a Propagating Dirichlet Process Mixture Model
,
2014,
IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[151]
Eleazar Eskin,et al.
Accurate viral population assembly from ultra-deep sequencing data
,
2014,
Bioinform..
[152]
T. Sharpton.
An introduction to the analysis of shotgun metagenomic data
,
2014,
Front. Plant Sci..
[153]
Gabor T. Marth,et al.
MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping
,
2013,
PloS one.
[154]
Christina A. Cuomo,et al.
Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement
,
2014,
PloS one.
[155]
M. Emond,et al.
Accuracy of Next Generation Sequencing Platforms.
,
2014,
Next generation, sequencing & applications.
[156]
Veli Mäkinen,et al.
Indexing Graphs for Path Queries with Applications in Genome Research
,
2014,
IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[157]
Ignacio Blanquer,et al.
Acceleration of short and long DNA read mapping without loss of accuracy using suffix array
,
2014,
Bioinform..
[158]
J. Wolf,et al.
A field guide to whole-genome sequencing, assembly and annotation
,
2014,
Evolutionary applications.
[159]
Justin Chu,et al.
DIDA: Distributed Indexing Dispatched Alignment
,
2015,
PloS one.
[160]
Steven L Salzberg,et al.
HISAT: a fast spliced aligner with low memory requirements
,
2015,
Nature Methods.
[161]
Pavel Skums,et al.
Antigenic cooperation among intrahost HCV variants organized into a complex network of cross-immunoreactivity
,
2015,
Proceedings of the National Academy of Sciences.
[162]
Mikhail Shugay,et al.
MiXCR: software for comprehensive adaptive immunity profiling
,
2015,
Nature Methods.
[163]
S. Lonardi,et al.
CLARK: fast and accurate classification of metagenomic and genomic sequences using discriminative k-mers
,
2015,
BMC Genomics.
[164]
Piotr Indyk,et al.
Edit Distance Cannot Be Computed in Strongly Subquadratic Time (unless SETH is false)
,
2014,
STOC.
[165]
N. Loman,et al.
A complete bacterial genome assembled de novo using only nanopore sequencing data
,
2015,
Nature Methods.
[166]
Sara Goodwin,et al.
Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome
,
2015,
bioRxiv.
[167]
Alexander Schönhuth,et al.
Characteristics of de novo structural changes in the human genome
,
2015,
Genome research.
[168]
Thomas Bonfert,et al.
ContextMap 2: fast and accurate context-based RNA-seq mapping
,
2015,
BMC Bioinformatics.
[169]
Chao Xie,et al.
Fast and sensitive protein alignment using DIAMOND
,
2014,
Nature Methods.
[170]
Jeroen Aerssens,et al.
VirVarSeq: a low-frequency virus variant detection pipeline for Illumina sequencing using adaptive base-calling accuracy filtering
,
2015,
Bioinform..
[171]
Yun Xu,et al.
BitMapper: an efficient all-mapper based on bit-vector computing
,
2015,
BMC Bioinformatics.
[172]
Christina Boucher,et al.
Misassembly detection using paired-end sequence reads and optical mapping data
,
2014,
Bioinform..
[173]
Heng Li,et al.
Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences
,
2015,
Bioinform..
[174]
Yadong Wang,et al.
rHAT: fast alignment of noisy long reads with regional hashing
,
2016,
Bioinform..
[175]
Onur Mutlu,et al.
Optimal seed solver: optimizing seed selection in read mapping
,
2015,
Bioinform..
[176]
Can Alkan,et al.
On genomic repeats and reproducibility
,
2016,
Bioinform..
[177]
Niranjan Nagarajan,et al.
Fast and sensitive mapping of nanopore sequencing reads with GraphMap
,
2016,
Nature Communications.
[178]
Robert Gentleman,et al.
Prediction and Quantification of Splice Events from RNA-Seq Data
,
2016,
PloS one.
[179]
David A. Matthews,et al.
Real-time, portable genome sequencing for Ebola surveillance
,
2016,
Nature.
[180]
Steven Skiena,et al.
NanoBLASTer: Fast alignment and characterization of Oxford Nanopore single molecule sequencing reads
,
2016,
2016 IEEE 6th International Conference on Computational Advances in Bio and Medical Sciences (ICCABS).
[181]
Alberto Policriti,et al.
Fast, accurate, and lightweight analysis of BS-treated reads with ERNE 2
,
2016,
BMC Bioinformatics.
[182]
Aaron Y. Lee,et al.
Scalable metagenomics alignment research tool (SMART): a scalable, rapid, and complete search heuristic for the classification of metagenomic sequences from complex sequence populations
,
2016,
BMC Bioinformatics.
[183]
Alexey I. Nesvizhskii,et al.
Two-pass alignment improves novel splice junction quantification
,
2015,
Bioinform..
[184]
E. S. Quintana-Ortí,et al.
Highly sensitive and ultrafast read mapping for RNA-seq analysis
,
2016,
DNA research : an international journal for rapid publication of reports on genes and genomes.
[185]
Lior Pachter,et al.
Near-optimal probabilistic RNA-seq quantification
,
2016,
Nature Biotechnology.
[186]
J. McPherson,et al.
Coming of age: ten years of next-generation sequencing technologies
,
2016,
Nature Reviews Genetics.
[187]
Bonnie Berger,et al.
Compressive mapping for next-generation sequencing
,
2016,
Nature Biotechnology.
[188]
Onur Mutlu,et al.
GateKeeper: a new hardware architecture for accelerating pre‐alignment in DNA short read mapping
,
2016,
Bioinform..
[189]
Steven L Salzberg,et al.
The first near-complete assembly of the hexaploid bread wheat genome, Triticum aestivum
,
2017,
bioRxiv.
[190]
Haris Vikalo,et al.
aBayesQR: A Bayesian Method for Reconstruction of Viral Populations Characterized by Low Diversity
,
2017,
RECOMB.
[191]
S. Koren,et al.
Nanopore sequencing and assembly of a human genome with ultra-long reads
,
2017,
bioRxiv.
[192]
Philip D. Blood,et al.
Critical Assessment of Metagenome Interpretation—a benchmark of metagenomics software
,
2017,
Nature Methods.
[193]
S. Koren,et al.
Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation
,
2016,
bioRxiv.
[194]
Kentaro K. Shimizu,et al.
Reference-guided de novo assembly approach improves genome reconstruction for related species
,
2017,
BMC Bioinformatics.
[195]
R. Durbin,et al.
Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
,
2016,
bioRxiv.
[196]
Eun Ji Kim,et al.
Simulation-based comprehensive benchmarking of RNA-seq aligners
,
2016,
Nature Methods.
[197]
Christos A. Ouzounis,et al.
Computational complexity of algorithms for sequence comparison, short-read assembly and genome alignment
,
2017,
Biosyst..
[198]
Piotr Wojtek Dabrowski,et al.
HiLive: real‐time mapping of illumina reads while sequencing
,
2016,
Bioinform..
[199]
Wen-Lian Hsu,et al.
Kart: a divide-and-conquer algorithm for NGS read alignment
,
2017,
Bioinform..
[200]
Johannes Söding,et al.
MMseqs2: sensitive protein sequence searching for the analysis of massive data sets
,
2017,
bioRxiv.
[201]
Deanna M. Church,et al.
Building and Improving Reference Genome Assemblies
,
2017,
Proceedings of the IEEE.
[202]
Eleazar Eskin,et al.
Long single-molecule reads can resolve the complexity of the Influenza virus composed of rare, closely related mutant variants
,
2016,
bioRxiv.
[203]
Michael Huber,et al.
MinVar: A rapid and versatile tool for HIV-1 drug resistance genotyping by deep sequencing.
,
2017,
Journal of virological methods.
[204]
C. Alkan,et al.
MAGNET: Understanding and Improving the Accuracy of Genome Pre-Alignment Filtering
,
2017,
1707.01631.
[205]
Shanrong Zhao,et al.
Evaluation and comparison of computational tools for RNA-seq isoform quantification
,
2017,
BMC Genomics.
[206]
Yadong Wang,et al.
LAMSA: fast split read alignment with long approximate matches
,
2017,
Bioinform..
[207]
Steven Salzberg,et al.
Short Read Mapping: An Algorithmic Tour
,
2017,
Proceedings of the IEEE.
[208]
David A. Eccles,et al.
De novo assembly of the complex genome of Nippostrongylus brasiliensis using MinION long reads
,
2018,
BMC Biology.
[209]
Rob Patro,et al.
Salmon provides fast and bias-aware quantification of transcript expression
,
2017,
Nature Methods.
[210]
Michael C. Schatz,et al.
Accurate detection of complex structural variations using single molecule sequencing
,
2017,
Nature Methods.
[211]
Alicia Oshlack,et al.
Necklace: combining reference and assembled transcriptomes for more comprehensive RNA-Seq analysis
,
2017,
bioRxiv.
[212]
Renan Valieris,et al.
Bioconda: sustainable and comprehensive software distribution for the life sciences
,
2018,
Nature Methods.
[213]
A. Battle,et al.
False positives in trans-eQTL and co-expression analyses arising from RNA-sequencing alignment errors
,
2018,
F1000Research.
[214]
Andreas Andrusch,et al.
DREAM‐Yara: an exact read mapper for very large databases with short update time
,
2018,
Bioinform..
[215]
Guoliang Li,et al.
An integrated package for bisulfite DNA methylation data analysis with Indel-sensitive mapping
,
2018,
BMC Bioinformatics.
[216]
Jean Thierry-Mieg,et al.
Magic-BLAST, an accurate DNA and RNA-seq aligner for long and short reads
,
2018,
bioRxiv.
[217]
Fritz J Sedlazeck,et al.
Piercing the dark matter: bioinformatics of long-range sequencing and mapping
,
2018,
Nature Reviews Genetics.
[218]
Wen-Lian Hsu,et al.
DART: a fast and accurate RNA-seq mapper with a partitioning strategy
,
2017,
Bioinform..
[219]
Yan Lu,et al.
A comprehensive evaluation of alignment software for reduced representation bisulfite sequencing data
,
2018,
Bioinform..
[220]
Justin Chu,et al.
Tigmint: correcting assembly errors using linked reads from large molecules
,
2018,
BMC Bioinformatics.
[221]
Adam M. Phillippy,et al.
MUMmer4: A fast and versatile genome alignment system
,
2018,
PLoS Comput. Biol..
[222]
Heng Li,et al.
Minimap2: pairwise alignment for nucleotide sequences
,
2017,
Bioinform..
[223]
William Jones,et al.
Variation graph toolkit improves read mapping by representing genetic variation in the reference
,
2018,
Nature Biotechnology.
[224]
C. Alkan,et al.
Hercules: a profile HMM-based hybrid error correction algorithm for long reads
,
2017,
bioRxiv.
[225]
Harianto Tjong,et al.
Picky Comprehensively Detects High Resolution Structural Variants in Nanopore Long Reads
,
2018,
Nature Methods.
[226]
Srinivas Aluru,et al.
A Fast Approximate Algorithm for Mapping Long Reads to Large Reference Databases
,
2017,
bioRxiv.
[227]
Onur Mutlu,et al.
GRIM-Filter: Fast seed location filtering in DNA read mapping using processing-in-memory technologies
,
2017,
BMC Genomics.
[228]
Brent S. Pedersen,et al.
Nanopore sequencing and assembly of a human genome with ultra-long reads
,
2017,
Nature Biotechnology.
[229]
Pavel Skums,et al.
Accurate assembly of minority viral haplotypes from next-generation sequencing through efficient noise reduction
,
2018,
bioRxiv.
[230]
Tam P. Sneddon,et al.
Long-read genome sequencing identifies causal structural variation in a Mendelian disease
,
2017,
Genetics in Medicine.
[231]
Evan E. Eichler,et al.
Long-read sequence and assembly of segmental duplications
,
2018,
Nature Methods.
[232]
Weiguo Liu,et al.
Fast and efficient short read mapping based on a succinct hash index
,
2018,
BMC Bioinformatics.
[233]
Min Zhao,et al.
The bioinformatics tools for the genome assembly and analysis based on third-generation sequencing.
,
2018,
Briefings in functional genomics.
[234]
Steven L Salzberg,et al.
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype
,
2019,
Nature Biotechnology.
[235]
Bertil Schmidt,et al.
BGSA: a bit-parallel global sequence alignment toolkit for multi-core and many-core architectures
,
2018,
Bioinform..
[236]
Sanghamitra Bandyopadhyay,et al.
conLSH: Context based Locality Sensitive Hashing for Mapping of noisy SMRT Reads
,
2019,
bioRxiv.
[237]
Jinyan Li,et al.
Index suffix-prefix overlaps by (w, k)-minimizer to generate long contigs for reads compression
,
2019,
Bioinform..
[238]
Alexander Payne,et al.
BulkVis: a graphical viewer for Oxford nanopore bulk FAST5 files
,
2018,
Bioinform..
[239]
Onur Mutlu,et al.
Shouji: a fast and efficient pre-alignment filter for sequence alignment
,
2018,
Bioinform..
[240]
Faraz Hach,et al.
lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data
,
2018,
Bioinform..
[241]
Sergey Koren,et al.
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome
,
2019,
Nature Biotechnology.
[242]
Mile Šikić,et al.
Graphmap2 - splice-aware RNA-seq mapper for long reads
,
2019,
bioRxiv.
[243]
B. Singer,et al.
A Practical Guide to the Measurement and Analysis of DNA Methylation.
,
2019,
American journal of respiratory cell and molecular biology.
[244]
Rajeev Balasubramonian,et al.
GenCache: Leveraging In-Cache Operators for Efficient Sequence Alignment
,
2019,
MICRO.
[245]
Bo Liu,et al.
deSALT: fast and accurate long transcriptomic read alignment with de Bruijn graph-based index
,
2019,
Genome Biology.
[246]
Veli Mäkinen,et al.
Bit-parallel sequence-to-graph alignment
,
2019,
Bioinform..
[247]
Yu Lin,et al.
Assembly of long, error-prone reads using repeat graphs
,
2018,
Nature Biotechnology.
[248]
Mick Watson,et al.
Errors in long-read assemblies can critically affect protein prediction
,
2019,
Nature Biotechnology.
[249]
Srinivas Aluru,et al.
Efficient Architecture-Aware Acceleration of BWA-MEM for Multicore Systems
,
2019,
2019 IEEE International Parallel and Distributed Processing Symposium (IPDPS).
[250]
William J. Dally,et al.
Darwin-WGA: A Co-processor Provides Increased Sensitivity in Whole Genome Alignments with High Speedup
,
2019,
2019 IEEE International Symposium on High Performance Computer Architecture (HPCA).
[251]
Jean Thierry-Mieg,et al.
Magic-BLAST, an accurate RNA-seq aligner for long and short reads
,
2019,
BMC Bioinformatics.
[252]
Fatemeh Almodaresi,et al.
Alignment and mapping methodology influence transcript abundance estimation
,
2020,
Genome biology.
[253]
Sanghamitra Bandyopadhyay,et al.
conLSH: Context based Locality Sensitive Hashing for mapping of noisy SMRT reads
,
2020,
Comput. Biol. Chem..
[254]
Telescope: an interactive tool for managing large-scale analysis from mobile devices
,
2019,
GigaScience.
[255]
Chaining with overlaps revisited
,
2020,
CPM.
[256]
Onur Mutlu,et al.
Apollo: A Sequencing-Technology-Independent, Scalable, and Accurate Assembly Polishing Algorithm
,
2019,
Bioinform..
[257]
Rachata Ausavarungnirun,et al.
GenASM: A High-Performance, Low-Power Approximate String Matching Acceleration Framework for Genome Sequence Analysis
,
2020,
2020 53rd Annual IEEE/ACM International Symposium on Microarchitecture (MICRO).
[258]
Onur Mutlu,et al.
Accelerating Genome Analysis: A Primer on an Ongoing Journey
,
2020,
IEEE Micro.
[259]
C. Alkan,et al.
SneakySnake: A Fast and Accurate Universal Genome Pre-Alignment Filter for CPUs, GPUs, and FPGAs
,
2019,
Bioinform..