Abstract
Guangjian Zeng, Chengzhi Zhao, Guanpeng Li, Zhengyang Huang, Jinhu Zhuang, Xiaohua Liang, Xiaxia Yu, Shenying Fang
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
europepmc
Confidence 96%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
No local reference links have been materialized yet.
10.1038/nature05610
10.1038/nature05610
10.1126/science.aab4082
10.1126/science.aab4082
10.1038/nrc2013
10.1038/nrc2013
10.1038/446145a
10.1038/446145a
10.1016/j.immuni.2018.03.023
10.1016/j.immuni.2018.03.023
10.1038/nrg2841
10.1038/nrg2841
10.1038/nature07943
10.1038/nature07943
An integrated map of genetic variation from 1,092 human genomes
10.1038/nature11632 · 2012
10.1038/nature11247
10.1038/nature11247
10.1038/s41586-020-2493-4
10.1038/s41586-020-2493-4
10.1093/nar/gky1015
10.1093/nar/gky1015
10.1093/nar/gkv1314
10.1093/nar/gkv1314
10.1007/s00439-013-1358-4
10.1007/s00439-013-1358-4
10.1093/database/bar026
10.1093/database/bar026
Oncokb: a precision oncology knowledge base
10.1200/po.17.00011 · 2017
10.1038/ng.2764
10.1038/ng.2764
Maxmif: a new method for identifying cancer driver genes through effective data integration
10.1002/advs.201800640 · 2018
10.1101/gr.134635.111
10.1101/gr.134635.111
10.1016/j.cell.2012.06.024
10.1016/j.cell.2012.06.024
10.1038/nature12912
10.1038/nature12912
10.1093/nar/gkz096
10.1093/nar/gkz096
10.1093/bioinformatics/bty511
10.1093/bioinformatics/bty511
Non-coding cancer driver candidates identified with a sample-and position-specific model of the somatic mutation rate
10.7554/elife.21778 · 2017
10.1158/0008-5472.can-09-1133
10.1158/0008-5472.can-09-1133
10.1093/bioinformatics/btaa242
10.1093/bioinformatics/btaa242
Ai-driver: an ensemble method for identifying driver mutations in personal cancer genomes
10.1093/nargab/lqaa084 · 2020
10.1093/nar/gkaa1033
10.1093/nar/gkaa1033
10.1093/bioinformatics/btu499
10.1093/bioinformatics/btu499
10.1093/bioinformatics/btt395
10.1093/bioinformatics/btt395
10.1016/j.cell.2018.02.060
10.1016/j.cell.2018.02.060
Deep learning for cancer type classification and driver gene identification
10.1186/s12859-021-04400-4 · 2021
Met exon 14 skipping: a case study for the detection of genetic variants in cancer driver genes by deep learning
10.3390/ijms22084217 · 2021
Deepallodriver: a deep learning-based strategy to predict cancer driver mutations
2023
10.1073/pnas.1616440113
10.1073/pnas.1616440113
Comprehensive assessment of computational algorithms in predicting cancer driver mutations
10.1186/s13059-020-01954-z · 2020
Unresolved referenced work
Kept as external metadata until matched
Integrating convolution and self-attention improves language model of human genome for interpreting non-coding regions at base-resolution
10.1093/nar/gkac326 · 2022
Language models are few-shot learners
2020
10.1038/s41568-018-0060-1
10.1038/s41568-018-0060-1
10.1038/nmeth.3547
10.1038/nmeth.3547
What's next for the ai protein-folding revolution
10.1038/d41586-022-00997-5 · doi-reference
10.1038/s41586-021-03819-2
10.1038/s41586-021-03819-2 · doi-reference
10.1126/science.adg7492
10.1126/science.adg7492 · doi-reference
10.1038/s41591-022-01981-2
10.1038/s41591-022-01981-2 · doi-reference
Identifying Mendelian disease genes with the variant effect scoring tool
10.1186/1471-2164-14-s3-s3 · doi-reference
10.1038/nprot.2015.123
10.1038/nprot.2015.123 · doi-reference
10.1093/nar/gkg509
10.1093/nar/gkg509 · doi-reference
10.1016/j.ajhg.2016.08.016
10.1016/j.ajhg.2016.08.016 · doi-reference
10.1371/journal.pone.0046688
10.1371/journal.pone.0046688 · doi-reference
10.1038/nmeth0410-248
10.1038/nmeth0410-248 · doi-reference
10.1371/journal.pone.0203553
10.1371/journal.pone.0203553 · doi-reference
10.1093/bioinformatics/btp528
10.1093/bioinformatics/btp528 · doi-reference
10.1038/nmeth.2890
10.1038/nmeth.2890 · doi-reference
10.1093/nar/gkr407
10.1093/nar/gkr407 · doi-reference
10.1101/148353
10.1101/148353 · doi-reference
10.1093/hmg/ddu733
10.1093/hmg/ddu733 · doi-reference
10.1038/ng.3703
10.1038/ng.3703 · doi-reference
10.1101/gr.092619.109
10.1101/gr.092619.109 · doi-reference
10.1038/ng.3196
10.1038/ng.3196 · doi-reference
A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data
10.1038/srep10576 · doi-reference
Fathmm-xf: accurate prediction of pathogenic point mutations via extended features
10.1093/bioinformatics/btx536 · doi-reference
10.1093/bioinformatics/btv009
10.1093/bioinformatics/btv009 · doi-reference
10.1093/bioinformatics/btt182
10.1093/bioinformatics/btt182 · doi-reference
Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models
10.1002/humu.22225 · doi-reference
10.1038/ng.3477
10.1038/ng.3477 · doi-reference
10.1093/nar/gkx390
10.1093/nar/gkx390 · doi-reference
Dann: a deep learning approach for annotating the pathogenicity of genetic variants
10.1093/bioinformatics/btu703 · doi-reference
10.1371/journal.pone.0077945
10.1371/journal.pone.0077945 · doi-reference
10.1093/nar/gky1016
10.1093/nar/gky1016 · doi-reference
10.1158/2159-8290.cd-16-0160
10.1158/2159-8290.cd-16-0160 · doi-reference
Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations
10.1186/s13059-014-0484-1 · doi-reference