Φορτώνει......
SNP and indel frequencies at transcription start sites and at canonical and alternative translation initiation sites in the human genome
Single-nucleotide polymorphisms (SNPs) are the most common form of genetic variation in humans and drive phenotypic variation. Due to evolutionary conservation, SNPs and indels (insertion and deletions) are depleted in functionally important sequence elements. Recently, population-scale sequencing e...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | PLoS One |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Public Library of Science
2019
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6461226/ https://ncbi.nlm.nih.gov/pubmed/30978217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0214816 |
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