Identifying Pathogenic Amino Acid Substitutions in Human Proteins Using Deep Learning
Many diseases of genetic origin originate from non-synonymous single nucleotide polymorphisms (nsSNPs). These cause changes in the final protein product encoded by a gene. Through large scale sequencing and population studies, there is growing availability of information of which variations are tole...
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| Format: | Others |
| Language: | English |
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KTH, Skolan för kemi, bioteknologi och hälsa (CBH)
2018
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| Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-233513 |