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GenomeVIP: a cloud platform for genomic variant discovery and interpretation
Identifying genomic variants is a fundamental first step toward the understanding of the role of inherited and acquired variation in disease. The accelerating growth in the corpus of sequencing data that underpins such analysis is making the data-download bottleneck more evident, placing substantial...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Genome Res |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Cold Spring Harbor Laboratory Press
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5538560/ https://ncbi.nlm.nih.gov/pubmed/28522612 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.211656.116 |
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