On the public citation graph
HTSlib-js: Developer toolkit for a client-side JavaScript interface for HTSlib
0 signed · 11 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1038/nature11632openalex-snapshot
An integrated map of genetic variation from 1,092 human genomes
inferredcites →https://doi.org/10.1038/nmeth.3174openalex-snapshot
bam.iobio: a web-based, real-time, sequence alignment file inspector
inferredcites →https://doi.org/10.1038/nmeth.3284openalex-snapshot
Digenome-seq: genome-wide profiling of CRISPR-Cas9 off-target effects in human cells
inferredcites →https://doi.org/10.1038/nmeth.4262openalex-snapshot
Digenome-seq web tool for profiling CRISPR specificity
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btr020openalex-snapshot
Dalliance: interactive genome viewing on the web
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/bioinformatics/btt314openalex-snapshot
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms
inferredcites →https://doi.org/10.1093/bioinformatics/btt750openalex-snapshot
Subclonal variant calling with multiple samples and prior knowledge
inferredcites →https://doi.org/10.1093/bioinformatics/btv098openalex-snapshot
Sambamba: fast processing of NGS alignment formats
inferredcites →https://doi.org/10.6084/m9.figshare.963153.v1openalex-snapshot
Aligning sequence reads, clone sequences and assembly con*gs with BWA-MEM
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