articleTop 1% cited
Strelka2: fast and accurate calling of germline and somatic variants
Nature Methods · 2018 · Vol. 15(8) · pp. 591–594
Sangtae Kim✉(Illumina (United States))Konrad Scheffler(Illumina (United States))Aaron L. Halpern(Illumina (United States))Mitchell A. Bekritsky(Illumina (United Kingdom))Eunho Noh(Illumina (United States))Morten Källberg(Illumina (United Kingdom))Xiaoyu Chen(Illumina (United States))Yeonbin Kim(Illumina (United States))Doruk Beyter(deCODE Genetics (Iceland))Peter Krusche(Illumina (United Kingdom))Christopher T. Saunders(Illumina (United States))
Cancer Genomics and DiagnosticsEpigenetics and DNA MethylationGenomics and Phylogenetic StudiesGermlineSomatic cellComputational biologyGermline mutationHaplotypeOpen sourceComputer scienceBiologySample (material)Genetics
MeSH terms
Whole Genome SequencingHaplotypesHumansModels, GeneticNeoplasmsSoftwareGenetic VariationGerm-Line MutationDatabases, GeneticINDEL MutationHigh-Throughput Nucleotide Sequencing
Citations
1,725
FWCI
40.51
field-weighted impact
References
15
Percentile
100%
vs. same field & year
Citations per year
References
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Genome Research · 2010 · 29,447 citations
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Nature Genetics · 2011 · 12,243 citations
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