Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experiments.
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| Title: | Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experiments. |
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| Authors: | Barbon L; Cancer, Ageing and Somatic Mutation Programme, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK., Offord V; Cancer, Ageing and Somatic Mutation Programme, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK., Radford EJ; Human Genetics Programme, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.; Department of Paediatrics, University of Cambridge, Cambridge CB2 0QQ, UK., Butler AP; Cancer, Ageing and Somatic Mutation Programme, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK., Gerety SS; Human Genetics Programme, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK., Adams DJ; Cancer, Ageing and Somatic Mutation Programme, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK., Tan HK; Human Genetics Programme, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK., Waters AJ; Cancer, Ageing and Somatic Mutation Programme, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK. |
| Source: | Bioinformatics (Oxford, England) [Bioinformatics] 2022 Jan 27; Vol. 38 (4), pp. 892-899. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Oxford University Press Country of Publication: England NLM ID: 9808944 Publication Model: Print Cited Medium: Internet ISSN: 1367-4811 (Electronic) Linking ISSN: 13674803 NLM ISO Abbreviation: Bioinformatics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1367-4811 |
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| DOI: | 10.1093/bioinformatics/btab776 |
