Versatile genome assembly evaluation with QUAST-LG
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Dmitry Antipov | Andrey D. Prjibelski | Alexey A. Gurevich | Vladislav Saveliev | Alla Mikheenko | A. Gurevich | A. Prjibelski | D. Antipov | V. Saveliev | Alla Mikheenko
[1] Heng Li,et al. Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences , 2015, Bioinform..
[2] Philip D. Blood,et al. Critical Assessment of Metagenome Interpretation—a benchmark of metagenomics software , 2017, Nature Methods.
[3] Christina A. Cuomo,et al. Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement , 2014, PloS one.
[4] Evgeny M. Zdobnov,et al. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs , 2015, Bioinform..
[5] Zhong Wang,et al. ALE: a generic assembly likelihood evaluation framework for assessing the accuracy of genome and metagenome assemblies , 2013, Bioinform..
[6] Niranjan Nagarajan,et al. Fast and accurate de novo genome assembly from long uncorrected reads. , 2017, Genome research.
[7] Pavel A. Pevzner,et al. Assembly of long error-prone reads using de Bruijn graphs , 2016, Proceedings of the National Academy of Sciences.
[8] Dmitry Antipov,et al. hybridSPAdes: an algorithm for hybrid assembly of short and long reads , 2016, Bioinform..
[9] Ryan M. Layer,et al. LUMPY: a probabilistic framework for structural variant discovery , 2012, Genome Biology.
[10] M. Schatz,et al. Algorithms Gage: a Critical Evaluation of Genome Assemblies and Assembly Material Supplemental , 2008 .
[11] Eugene W. Myers,et al. Chaining multiple-alignment fragments in sub-quadratic time , 1995, SODA '95.
[12] Mark J. P. Chaisson,et al. De novo fragment assembly with short mate-paired reads: Does the read length matter? , 2009, Genome research.
[13] Daniel Mapleson,et al. KAT: a K-mer analysis toolkit to quality control NGS datasets and genome assemblies , 2016, bioRxiv.
[14] Alexey A. Gurevich,et al. MetaQUAST: evaluation of metagenome assemblies , 2016, Bioinform..
[15] Jian Wang,et al. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler , 2012, GigaScience.
[16] David Tse,et al. Optimal assembly for high throughput shotgun sequencing , 2013, BMC Bioinformatics.
[17] Steven Salzberg,et al. GAGE-B: an evaluation of genome assemblers for bacterial organisms , 2013, Bioinform..
[18] Sebastian Deorowicz,et al. KMC 3: counting and manipulating k‐mer statistics , 2017, Bioinform..
[19] Michael Roberts,et al. The MaSuRCA genome assembler , 2013, Bioinform..
[20] Tetsuya Hayashi,et al. Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads , 2014, Genome research.
[21] Andrey D. Prjibelski,et al. Assembling short reads from jumping libraries with large insert sizes , 2015, Bioinform..
[22] Isaac Y. Ho,et al. Meraculous: De Novo Genome Assembly with Short Paired-End Reads , 2011, PloS one.
[23] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[24] Enno Ohlebusch,et al. Chaining algorithms for multiple genome comparison , 2005, J. Discrete Algorithms.
[25] Mark J. P. Chaisson,et al. Resolving the complexity of the human genome using single-molecule sequencing , 2014, Nature.
[26] Joachim Weischenfeldt,et al. SvABA: genome-wide detection of structural variants and indels by local assembly , 2018, Genome research.
[27] Yu Lin,et al. Assembly of long, error-prone reads using repeat graphs , 2018, Nature Biotechnology.
[28] Yu Lin,et al. Assembly of long, error-prone reads using repeat graphs , 2018, Nature Biotechnology.
[29] S. Salzberg,et al. Versatile and open software for comparing large genomes , 2004, Genome Biology.
[30] Andrey D. Prjibelski,et al. Icarus: visualizer for de novo assembly evaluation , 2016, Bioinform..
[31] A. Gnirke,et al. High-quality draft assemblies of mammalian genomes from massively parallel sequence data , 2010, Proceedings of the National Academy of Sciences.
[32] Heng Li. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.
[33] M. Schatz,et al. Phased diploid genome assembly with single-molecule real-time sequencing , 2016, Nature Methods.
[34] S. Koren,et al. Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation , 2016, bioRxiv.
[35] S. Koren,et al. Assembly algorithms for next-generation sequencing data. , 2010, Genomics.
[36] Inanç Birol,et al. Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species , 2013, GigaScience.
[37] Steven J. M. Jones,et al. Circos: an information aesthetic for comparative genomics. , 2009, Genome research.
[38] Daniel D. Sommer,et al. De novo likelihood-based measures for comparing genome assemblies , 2013, BMC Research Notes.
[39] M. Berriman,et al. REAPR: a universal tool for genome assembly evaluation , 2013, Genome Biology.
[40] Sergey I. Nikolenko,et al. SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing , 2012, J. Comput. Biol..
[41] Alexey A. Gurevich,et al. QUAST: quality assessment tool for genome assemblies , 2013, Bioinform..
[42] Eugene Goltsman,et al. Meraculous2: fast accurate short-read assembly of large polymorphic genomes , 2016, ArXiv.
[43] Nuno A. Fonseca,et al. Assemblathon 1: a competitive assessment of de novo short read assembly methods. , 2011, Genome research.
[44] Brendan L. O’Connell,et al. Chromosome-scale shotgun assembly using an in vitro method for long-range linkage , 2015, Genome research.
[45] Walter Pirovano,et al. SSPACE-LongRead: scaffolding bacterial draft genomes using long read sequence information , 2014, BMC Bioinformatics.
[46] Lars Arvestad,et al. BESST - Efficient scaffolding of large fragmented assemblies , 2014, BMC Bioinformatics.
[47] Michael Roberts,et al. Reducing storage requirements for biological sequence comparison , 2004, Bioinform..
[48] David Tse,et al. Near-optimal assembly for shotgun sequencing with noisy reads , 2014, BMC Bioinformatics.
[49] Alexa B. R. McIntyre,et al. Extensive sequencing of seven human genomes to characterize benchmark reference materials , 2015, Scientific Data.
[50] Ole Schulz-Trieglaff,et al. NxTrim: optimized trimming of Illumina mate pair reads , 2014, bioRxiv.
[51] Justin Chu,et al. ABySS 2.0: resource-efficient assembly of large genomes using a Bloom filter , 2016, bioRxiv.
[52] Heng Li,et al. Minimap2: fast pairwise alignment for long nucleotide sequences , 2017 .
[53] Hani Z. Girgis. Red: an intelligent, rapid, accurate tool for detecting repeats de-novo on the genomic scale , 2015, BMC Bioinformatics.
[54] Lars Feuk,et al. The Database of Genomic Variants: a curated collection of structural variation in the human genome , 2013, Nucleic Acids Res..
[55] Adam M. Phillippy,et al. MUMmer4: A fast and versatile genome alignment system , 2018, PLoS Comput. Biol..
[56] M. Borodovsky,et al. Gene identification in novel eukaryotic genomes by self-training algorithm , 2005, Nucleic acids research.