Á lódáil...
The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection
With the development of High-Throughput Sequencing (HTS) thousands of human genomes have now been sequenced. Whenever different studies analyze the same genome they usually agree on the amount of single-nucleotide polymorphisms, but differ dramatically on the number of insertion and deletion variant...
Na minha lista:
| Foilsithe in: | Nucleic Acids Res |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4551921/ https://ncbi.nlm.nih.gov/pubmed/26130710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv677 |
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