Accurate genomic variant detection in single cells with primary template-directed amplification is a research paper published in Proceedings of the National Academy of Sciences (2021). On theSindex it has a DataRank of 0. It has been cited 193 times.
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HHS | National Institutes of Health
Grant: 1DP2CA239145
Burroughs Wellcome Fund
Grant: CAMS
ALSAC
Grant: St. Jude Funding
Hyundai Foundation for Pediatric Reseaerch
Grant: Scholar
European Hematology Association
Grant: TRTH75
NCI NIH HHS
Grant: DP2 CA239145
NCI NIH HHS
Grant: L40 CA162153
FWCI
8.98
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 1 of Construction of high coverage whole-genome sequencing libraries from single colon crypts without DNA extraction or whole-genome amplification
Additional file 1 of Construction of high coverage whole-genome sequencing libraries from single colon crypts without DNA extraction or whole-genome amplification
Additional file 1 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 1 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 5 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 5 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 4 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 3 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 2 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 3 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 2 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics
Additional file 4 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics