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GTB – an online genome tolerance browser
BACKGROUND: Accurate methods capable of predicting the impact of single nucleotide variants (SNVs) are assuming ever increasing importance. There exists a plethora of in silico algorithms designed to help identify and prioritize SNVs across the human genome for further investigation. However, no too...
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/PMC5219737/ https://ncbi.nlm.nih.gov/pubmed/28061747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-1436-4 |
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