grch37

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Identify which human reference genome was used to align a BAM/SAM/CRAM file

rust bioinformatics genomics sam bam reference-genome cram hg19 grch37 grch38 hg38

UniProt genome annotation data in hg19/GRCh37 coordinates

annotation genome uniprotkb hg19 grch37

Identification of cancer-causing variants

Code for webscraping details about SNPs using RS IDs from dbSNP

mutation dbsnp webscraping ncbi grch37 grch38

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