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Pysim-sv: a package for simulating structural variation data with GC-biases
BACKGROUND: Structural variations (SVs) are wide-spread in human genomes and may have important implications in disease-related and evolutionary studies. High-throughput sequencing (HTS) has become a major platform for SV detection and simulation serves as a powerful and cost-effective approach for...
Tallennettuna:
| Julkaisussa: | BMC Bioinformatics |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5374556/ https://ncbi.nlm.nih.gov/pubmed/28361688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1464-8 |
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