Gabor T Marth

Author PubWeight™ 172.36‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
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