Pacybara: accurate long-read sequencing for barcoded mutagenized allelic libraries is a research paper published in Bioinformatics (2024). On theSindex it has a DataRank of 0. It has been cited 8 times.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
NIGMS NIH HHS
Grant: R01 GM132162
NHLBI NIH HHS
Grant: R01 HL164675
Canadian Institutes of Health Research
Grant: unidentified
unidentified
National Institutes of Health
Grant: 1UM1HG011969-01
The Center for Actionable Variant Analysis; measuring variant function at scale
National Institutes of Health
Grant: 1R01HL164675-01
Systematically mapping variant effects for cardiovascular genes
National Institutes of Health
Grant: 5UM1HG011989-02
Molecular phenotyping of ~100,000 coding variants across Mendelian disease genes
National Institutes of Health
Grant: 5R35GM133428-04
Investigating the landscape and genetic architecture of germline mutagenesis
National Institutes of Health
Grant: 5R01GM132162-03
Comprehensive, context-aware, functional analysis of Cytochrome P450 variants
National Institutes of Health
Grant: 5RM1HG010461-05
Center for the Multiplexed Assessment of Phenotype
National Human Genome Research Institute
NIH HHS
National Institutes of Health
FWCI
3.47
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords