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come on work darnit
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mathiasbio committed Oct 17, 2024
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#. **Cancer genomics workflow**: MGI's CWL Cancer Pipelines. https://github.com/genome/cancer-genomics-workflow/wiki
#. **GIAB**: The priority of GIAB is authoritative characterization of human genomes for use in analytical validation and technology development, optimization, and demonstration. https://github.com/genome-in-a-bottle
#. **dbNSFP**: dbNSFP is a database developed for functional prediction and annotation of all potential non-synonymous single-nucleotide variants (nsSNVs) in the human genome. https://sites.google.com/site/jpopgen/dbNSFP
#. **1000Genomes**: The goal of the 1000 Genomes Project was to find most genetic variants with frequencies of at least 1% in the populations studied. https://www.internationalgenome.org/about Download link: https://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/
#. **1000Genomes**: The goal of the 1000 Genomes Project was to find most genetic variants with frequencies of at least 1% in the populations studied. https://www.internationalgenome.org/ Download link: https://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/
#. **HapMap3**: The International HapMap Project was an organization that aimed to develop a haplotype map (HapMap) of the human genome, to describe the common patterns of human genetic variation. HapMap 3 is the third phase of the International HapMap project. http://www.sanger.ac.uk/resources/downloads/human/hapmap3.html Download link: ftp://ftp.ncbi.nlm.nih.gov/hapmap/
#. **GRCh38.p11**: GRCh38.p11 is the eleventh patch release for the GRCh38 (human) reference assembly. https://www.ncbi.nlm.nih.gov/grc/human Download link: ftp://ftp.ncbi.nlm.nih.gov/genomes/all/GCA/000/001/405/
#. **dbVar**: dbVar is NCBI's database of genomic structural variation – insertions, deletions, duplications, inversions, mobile element insertions, translocations, and complex chromosomal rearrangements https://www.ncbi.nlm.nih.gov/dbvar Download link: https://www.ncbi.nlm.nih.gov/dbvar/content/ftp_manifest/
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