The variant call format and VCFtools is a research paper published in Bioinformatics (2011). On theSindex it has a DataRank of 1.5. It has been cited 17,436 times.
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Base Score Contribution
1.5
From this paper's citation signal
Citation Network Contribution
0
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Learn more about DataRank methodology →NHGRI NIH HHS
Grant: U01 HG005208
British Heart Foundation
Grant: RG/09/012/28096
Wellcome Trust
Grant: 090532
Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics.
Medical Research Council
Grant: G0801056B
Wellcome Trust
Grant: 086084
NHGRI NIH HHS
Grant: R01 HG004719
NHGRI NIH HHS
Grant: 54 HG003067
Wellcome Trust
Grant: 075491/Z/04
National Institutes of Health
Grant: 3U54HG003067-07S1
Large Scale Sequencing and Analysis of Genomes
National Institutes of Health
Grant: 5R01HG004719-02
Software Tools for Next-Generation Sequencer Data
National Institutes of Health
Grant: 3U01HG005208-02S1
Joint SNP and CNV calling in 1000 Genomes sequence data
Intramural NIH HHS
Fields of Study
MeSH Terms
Keywords
From Relative Compression to Hierarchical Compression
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Additional file 4 of An efficient CRISPR-Cas9 enrichment sequencing strategy for characterizing complex and highly duplicated genomic regions. A case study in the Prunus salicina LG3-MYB10 genes cluster
Additional file 4 of An efficient CRISPR-Cas9 enrichment sequencing strategy for characterizing complex and highly duplicated genomic regions. A case study in the Prunus salicina LG3-MYB10 genes cluster
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