Suppr超能文献

相似文献

1
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.
Science. 2015 May 8;348(6235):666-9. doi: 10.1126/science.1261877.
2
The Characteristics of Heterozygous Protein Truncating Variants in the Human Genome.
PLoS Comput Biol. 2015 Dec 7;11(12):e1004647. doi: 10.1371/journal.pcbi.1004647. eCollection 2015 Dec.
3
Nonsense-mediated decay is highly stable across individuals and tissues.
Am J Hum Genet. 2021 Aug 5;108(8):1401-1408. doi: 10.1016/j.ajhg.2021.06.008. Epub 2021 Jul 2.
4
Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.
Science. 2015 May 8;348(6235):648-60. doi: 10.1126/science.1262110. Epub 2015 May 7.
5
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report.
J Med Genet. 2019 Jul;56(7):453-460. doi: 10.1136/jmedgenet-2018-105834. Epub 2019 Mar 19.
6
Human genomics. The human transcriptome across tissues and individuals.
Science. 2015 May 8;348(6235):660-5. doi: 10.1126/science.aaa0355.
7
9
10
Human genetics. GTEx detects genetic effects.
Science. 2015 May 8;348(6235):640-1. doi: 10.1126/science.aab3002.

引用本文的文献

1
Deep Brain Stimulation in Leigh-Like Syndrome Due to DNM1 Pathogenic Variant.
Tremor Other Hyperkinet Mov (N Y). 2025 Jul 22;15:32. doi: 10.5334/tohm.1017. eCollection 2025.
2
ASET: An end-to-end pipeline for quantification and visualization of allele specific expression.
Res Sq. 2025 Jun 13:rs.3.rs-6844336. doi: 10.21203/rs.3.rs-6844336/v1.
4
An engineered glutamic acid tRNA for efficient suppression of pathogenic nonsense mutations.
Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf532.
8
Bayesian estimation of allele-specific expression in the presence of phasing uncertainty.
Bioinformatics. 2025 Jun 2;41(6). doi: 10.1093/bioinformatics/btaf283.
9
GDC: Integration of Multi-Omic and Phenotypic Resources to Unravel the Genetic Pathogenesis of Hearing Loss.
Adv Sci (Weinh). 2025 Aug;12(29):e2408891. doi: 10.1002/advs.202408891. Epub 2025 Mar 16.

本文引用的文献

1
Choice of transcripts and software has a large effect on variant annotation.
Genome Med. 2014 Mar 31;6(3):26. doi: 10.1186/gm543. eCollection 2014.
2
Allelic expression of deleterious protein-coding variants across human tissues.
PLoS Genet. 2014 May 1;10(5):e1004304. doi: 10.1371/journal.pgen.1004304. eCollection 2014 May.
3
Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencing.
Nat Methods. 2014 Jan;11(1):51-4. doi: 10.1038/nmeth.2736. Epub 2013 Nov 24.
5
Transcriptome and genome sequencing uncovers functional variation in humans.
Nature. 2013 Sep 26;501(7468):506-11. doi: 10.1038/nature12531. Epub 2013 Sep 15.
7
The Genotype-Tissue Expression (GTEx) project.
Nat Genet. 2013 Jun;45(6):580-5. doi: 10.1038/ng.2653.
8
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.
Genome Res. 2013 May;23(5):749-61. doi: 10.1101/gr.148718.112. Epub 2013 Mar 11.
9
A systematic survey of loss-of-function variants in human protein-coding genes.
Science. 2012 Feb 17;335(6070):823-8. doi: 10.1126/science.1215040.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验