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Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel
BACKGROUND: Recent advances in molecular genetic analysis using next‐generation sequencing (NGS) have drastically accelerated the identification of disease‐causing gene mutations. Most next‐generation sequencing analyses of inherited diseases have mainly focused on single‐nucleotide variants and sho...
में बचाया:
| में प्रकाशित: | Mol Genet Genomic Med |
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| मुख्य लेखकों: | , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
John Wiley and Sons Inc.
2018
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6081219/ https://ncbi.nlm.nih.gov/pubmed/29633566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.399 |
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