1
|
An integrated map of genetic variation from 1,092 human genomes.
|
Nature
|
2012
|
59.82
|
2
|
Whole-genome sequencing and variant discovery in C. elegans.
|
Nat Methods
|
2008
|
31.92
|
3
|
The variant call format and VCFtools.
|
Bioinformatics
|
2011
|
25.88
|
4
|
Mapping copy number variation by population-scale genome sequencing.
|
Nature
|
2011
|
12.55
|
5
|
Rapid whole-genome mutational profiling using next-generation sequencing technologies.
|
Genome Res
|
2008
|
8.01
|
6
|
A standard variation file format for human genome sequences.
|
Genome Biol
|
2010
|
7.83
|
7
|
Demographic history and rare allele sharing among human populations.
|
Proc Natl Acad Sci U S A
|
2011
|
7.36
|
8
|
ART: a next-generation sequencing read simulator.
|
Bioinformatics
|
2011
|
5.13
|
9
|
BamTools: a C++ API and toolkit for analyzing and managing BAM files.
|
Bioinformatics
|
2011
|
3.59
|
10
|
A comprehensive map of mobile element insertion polymorphisms in humans.
|
PLoS Genet
|
2011
|
3.14
|
11
|
Primer-site SNPs mask mutations.
|
Nat Methods
|
2007
|
1.83
|
12
|
SSW library: an SIMD Smith-Waterman C/C++ library for use in genomic applications.
|
PLoS One
|
2013
|
1.40
|
13
|
Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogaster.
|
Genome Biol Evol
|
2009
|
1.36
|
14
|
Scotty: a web tool for designing RNA-Seq experiments to measure differential gene expression.
|
Bioinformatics
|
2013
|
1.26
|
15
|
A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosis.
|
Science
|
2012
|
1.24
|
16
|
SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization.
|
Genome Biol
|
2014
|
1.12
|
17
|
Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data.
|
BMC Bioinformatics
|
2012
|
1.09
|
18
|
Extending reference assembly models.
|
Genome Biol
|
2015
|
1.06
|
19
|
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences.
|
Genome Biol
|
2014
|
0.98
|
20
|
Targeted proteomic dissection of Toxoplasma cytoskeleton sub-compartments using MORN1.
|
Cytoskeleton (Hoboken)
|
2012
|
0.97
|
21
|
Analysis of concordance of different haplotype block partitioning algorithms.
|
BMC Bioinformatics
|
2005
|
0.94
|
22
|
Expression divergence measured by transcriptome sequencing of four yeast species.
|
BMC Genomics
|
2011
|
0.91
|
23
|
Whole genome profiling of spontaneous and chemically induced mutations in Toxoplasma gondii.
|
BMC Genomics
|
2014
|
0.89
|
24
|
Genetic basis for phenotypic differences between different Toxoplasma gondii type I strains.
|
BMC Genomics
|
2013
|
0.88
|
25
|
Variant discovery in targeted resequencing using whole genome amplified DNA.
|
BMC Genomics
|
2013
|
0.77
|