The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
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M. DePristo | E. Banks | K. Garimella | M. Hanna | A. McKenna | A. Kernytsky | A. Sivachenko | K. Cibulskis | S. Gabriel | D. Altshuler | M. Daly
[1] B. Weir,et al. Bayesian statistics in genetics: a guide for the uninitiated. , 1999, Trends in genetics : TIG.
[2] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[3] J. Mullikin,et al. SSAHA: a fast search method for large DNA databases. , 2001, Genome research.
[4] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[5] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[6] Sophie Palmer,et al. Complete MHC haplotype sequencing for common disease gene mapping. , 2004, Genome research.
[7] Sanjay Ghemawat,et al. MapReduce: Simplified Data Processing on Large Clusters , 2004, OSDI.
[8] James R. Knight,et al. Genome sequencing in microfabricated high-density picolitre reactors , 2005, Nature.
[9] Pardis C Sabeti,et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC , 2006, Nature Genetics.
[10] J. Lupski,et al. The complete genome of an individual by massively parallel DNA sequencing , 2008, Nature.
[11] Hanlee P. Ji,et al. Next-generation DNA sequencing , 2008, Nature Biotechnology.
[12] Antony V. Cox,et al. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing , 2008, Nature Genetics.
[13] Ruiqiang Li,et al. SOAP: short oligonucleotide alignment program , 2008, Bioinform..
[14] Nancy F. Hansen,et al. Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry , 2008, Nature.
[15] Joshua M. Korn,et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs , 2008, Nature Genetics.
[16]
R. Durbin,et al.
Mapping Quality Scores Mapping Short Dna Sequencing Reads and Calling Variants Using P ,
2022
.
[17]
Dawei Li,et al.
The diploid genome sequence of an Asian individual
,
2008,
Nature.
[18]
A. Mortazavi,et al.
Computation for ChIP-seq and RNA-seq studies
,
2009,
Nature Methods.
[19]
Francisco M. De La Vega,et al.
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.
,
2009,
Genome research.
[20]
J. Maguire,et al.
Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing
,
2009,
Nature Biotechnology.
[21]
Yuriy Fofanov,et al.
PIQA: pipeline for Illumina G1 genome analyzer data quality assessment
,
2009,
Bioinform..
[22]
Gonçalo R. Abecasis,et al.
The Sequence Alignment/Map format and SAMtools
,
2009,
Bioinform..
[23]
Richard Durbin,et al.
Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform
,
2009
.
[24]
R. Wilson,et al.
BreakDancer: An algorithm for high resolution mapping of genomic structural variation
,
2009,
Nature Methods.
[25]
Ken Chen,et al.
VarScan: variant detection in massively parallel sequencing of individual and pooled samples
,
2009,
Bioinform..
[26]
Robert Gentleman,et al.
ShortRead: a bioconductor package for input, quality assessment and exploration of high-throughput sequence data
,
2009,
Bioinform..
[27]
Robert B. Hartlage,et al.
This PDF file includes: Materials and Methods
,
2009
.