Please use this identifier to cite or link to this item:
https://doi.org/10.1186/gb-2012-13-2-r9
DC Field | Value | |
---|---|---|
dc.title | Predicting the effects of frameshifting indels | |
dc.contributor.author | Hu, J | |
dc.contributor.author | Ng, P.C | |
dc.date.accessioned | 2020-11-10T00:37:05Z | |
dc.date.available | 2020-11-10T00:37:05Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | Hu, J, Ng, P.C (2012). Predicting the effects of frameshifting indels. Genome Biology 13 (2) : R9. ScholarBank@NUS Repository. https://doi.org/10.1186/gb-2012-13-2-r9 | |
dc.identifier.issn | 14747596 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/183237 | |
dc.description.abstract | Each human has approximately 50 to 280 frameshifting indels, yet their implications are unknown. We created SIFT Indel, a prediction method for frameshifting indels that has 84% accuracy. The percentage of human frameshifting indels predicted to be gene-damaging is negatively correlated with allele frequency. We also show that although the first frameshifting indel in a gene causes loss of function, there is a tendency for the second frameshifting indel to compensate and restore protein function. SIFT Indel is available at http://sift-dna.org/www/SIFT_indels2.html. © 2012 Hu and Ng; licensee BioMed Central Ltd. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | complementary DNA | |
dc.subject | DNA | |
dc.subject | protein | |
dc.subject | accuracy | |
dc.subject | African | |
dc.subject | article | |
dc.subject | Asian | |
dc.subject | classification algorithm | |
dc.subject | classifier | |
dc.subject | CYP3A gene | |
dc.subject | decision tree | |
dc.subject | DNA sequence | |
dc.subject | ethnic group | |
dc.subject | European | |
dc.subject | exon | |
dc.subject | frameshifting indel | |
dc.subject | gene | |
dc.subject | gene cluster | |
dc.subject | gene deletion | |
dc.subject | gene frequency | |
dc.subject | gene function | |
dc.subject | gene insertion | |
dc.subject | genetic conservation | |
dc.subject | HERC2 gene | |
dc.subject | human | |
dc.subject | human genome | |
dc.subject | intron | |
dc.subject | nonhuman | |
dc.subject | protein function | |
dc.subject | sensitivity and specificity | |
dc.subject | sequence alignment | |
dc.subject | SIFT indel algorithm | |
dc.subject | algorithm | |
dc.subject | animal | |
dc.subject | biology | |
dc.subject | Caucasian | |
dc.subject | computer program | |
dc.subject | frameshift mutation | |
dc.subject | genetics | |
dc.subject | indel mutation | |
dc.subject | Negro | |
dc.subject | African Continental Ancestry Group | |
dc.subject | Algorithms | |
dc.subject | Animals | |
dc.subject | Asian Continental Ancestry Group | |
dc.subject | Computational Biology | |
dc.subject | European Continental Ancestry Group | |
dc.subject | Frameshift Mutation | |
dc.subject | Gene Frequency | |
dc.subject | Genome, Human | |
dc.subject | Humans | |
dc.subject | INDEL Mutation | |
dc.subject | Proteins | |
dc.subject | Software | |
dc.type | Article | |
dc.contributor.department | MEDICINE | |
dc.description.doi | 10.1186/gb-2012-13-2-r9 | |
dc.description.sourcetitle | Genome Biology | |
dc.description.volume | 13 | |
dc.description.issue | 2 | |
dc.description.page | R9 | |
Appears in Collections: | Staff Publications Elements |
Show simple item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_1186_gb-2012-13-2-r9.pdf | 991.07 kB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License