SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing is a research paper published in Frontiers in Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 19 times.
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National Institutes of Health
Grant: P01 AG017242
National Institutes of Health
Grant: P01 AG047200
National Institutes of Health
Grant: P30 AG038072
National Institutes of Health
Grant: K99 AG056656
National Institutes of Health
Grant: the Paul F. Glenn Center for the Biology of Human Aging
National Institutes of Health
Grant: U01 ES029519
National Institutes of Health
Grant: U19 AG056278
National Institutes of Health
Grant: U01 HL145560
FWCI
0.78
Citation Percentile
0.7%
Citation Trend
Fields of Study
Keywords