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Bioinformatics Interpretation of Exome Sequencing: Blood Cancer
We had analyzed 10 exome sequencing data and single nucleotide polymorphism chips for blood cancer provided by the PGM21 (The National Project for Personalized Genomic Medicine) Award program. We had removed sample G06 because the pair is not correct and G10 because of possible contamination. In-hou...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korea Genome Organization
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3630382/ https://ncbi.nlm.nih.gov/pubmed/23613679 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2013.11.1.24 |
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