188 related articles for article (PubMed ID: 36410474)
1. Mapping the Constrained Coding Regions in the Human Genome to Their Corresponding Proteins.
Hasenahuer MA; Sanchis-Juan A; Laskowski RA; Baker JA; Stephenson JD; Orengo CA; Raymond FL; Thornton JM
J Mol Biol; 2023 Jan; 435(2):167892. PubMed ID: 36410474
[TBL] [Abstract][Full Text] [Related]
2. A map of constrained coding regions in the human genome.
Havrilla JM; Pedersen BS; Layer RM; Quinlan AR
Nat Genet; 2019 Jan; 51(1):88-95. PubMed ID: 30531870
[TBL] [Abstract][Full Text] [Related]
3. A genomic mutational constraint map using variation in 76,156 human genomes.
Chen S; Francioli LC; Goodrich JK; Collins RL; Kanai M; Wang Q; Alföldi J; Watts NA; Vittal C; Gauthier LD; Poterba T; Wilson MW; Tarasova Y; Phu W; Grant R; Yohannes MT; Koenig Z; Farjoun Y; Banks E; Donnelly S; Gabriel S; Gupta N; Ferriera S; Tolonen C; Novod S; Bergelson L; Roazen D; Ruano-Rubio V; Covarrubias M; Llanwarne C; Petrillo N; Wade G; Jeandet T; Munshi R; Tibbetts K; ; O'Donnell-Luria A; Solomonson M; Seed C; Martin AR; Talkowski ME; Rehm HL; Daly MJ; Tiao G; Neale BM; MacArthur DG; Karczewski KJ
Nature; 2024 Jan; 625(7993):92-100. PubMed ID: 38057664
[TBL] [Abstract][Full Text] [Related]
4. Analysis of genomic variation in non-coding elements using population-scale sequencing data from the 1000 Genomes Project.
Mu XJ; Lu ZJ; Kong Y; Lam HY; Gerstein MB
Nucleic Acids Res; 2011 Sep; 39(16):7058-76. PubMed ID: 21596777
[TBL] [Abstract][Full Text] [Related]
5. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
Zhang DL; Ji L; Li YD
Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
[TBL] [Abstract][Full Text] [Related]
6. 8.2% of the Human genome is constrained: variation in rates of turnover across functional element classes in the human lineage.
Rands CM; Meader S; Ponting CP; Lunter G
PLoS Genet; 2014 Jul; 10(7):e1004525. PubMed ID: 25057982
[TBL] [Abstract][Full Text] [Related]
7. Comparison of RefSeq protein-coding regions in human and vertebrate genomes.
Fong JH; Murphy TD; Pruitt KD
BMC Genomics; 2013 Sep; 14():654. PubMed ID: 24063302
[TBL] [Abstract][Full Text] [Related]
8. Small open reading frames: a comparative genetics approach to validation.
Jain N; Richter F; Adzhubei I; Sharp AJ; Gelb BD
BMC Genomics; 2023 May; 24(1):226. PubMed ID: 37127568
[TBL] [Abstract][Full Text] [Related]
9. Amino acids as placeholders: base-composition pressures on protein length in malaria parasites and prokaryotes.
Rayment JH; Forsdyke DR
Appl Bioinformatics; 2005; 4(2):117-30. PubMed ID: 16128613
[TBL] [Abstract][Full Text] [Related]
10. Exhaustive prediction of disease susceptibility to coding base changes in the human genome.
Kulkarni V; Errami M; Barber R; Garner HR
BMC Bioinformatics; 2008 Aug; 9 Suppl 9(Suppl 9):S3. PubMed ID: 18793467
[TBL] [Abstract][Full Text] [Related]
11. SNPs occur in regions with less genomic sequence conservation.
Castle JC
PLoS One; 2011; 6(6):e20660. PubMed ID: 21674007
[TBL] [Abstract][Full Text] [Related]
12. Prot2HG: a database of protein domains mapped to the human genome.
Stanek D; Bis-Brewer DM; Saghira C; Danzi MC; Seeman P; Lassuthova P; Zuchner S
Database (Oxford); 2020 Jan; 2020():. PubMed ID: 32293014
[TBL] [Abstract][Full Text] [Related]
13. The human noncoding genome defined by genetic diversity.
di Iulio J; Bartha I; Wong EHM; Yu HC; Lavrenko V; Yang D; Jung I; Hicks MA; Shah N; Kirkness EF; Fabani MM; Biggs WH; Ren B; Venter JC; Telenti A
Nat Genet; 2018 Mar; 50(3):333-337. PubMed ID: 29483654
[TBL] [Abstract][Full Text] [Related]
14. Deep sequencing of 10,000 human genomes.
Telenti A; Pierce LC; Biggs WH; di Iulio J; Wong EH; Fabani MM; Kirkness EF; Moustafa A; Shah N; Xie C; Brewerton SC; Bulsara N; Garner C; Metzker G; Sandoval E; Perkins BA; Och FJ; Turpaz Y; Venter JC
Proc Natl Acad Sci U S A; 2016 Oct; 113(42):11901-11906. PubMed ID: 27702888
[TBL] [Abstract][Full Text] [Related]
15. Evolutionary conservation in noncoding genomic regions.
Leypold NA; Speicher MR
Trends Genet; 2021 Oct; 37(10):903-918. PubMed ID: 34238591
[TBL] [Abstract][Full Text] [Related]
16. Annotation of 1350 Common Genetic Variants of the 19 ALDH Multigene Family from Global Human Genome Aggregation Database (gnomAD).
Chen CH; Kraemer BR; Lee L; Mochly-Rosen D
Biomolecules; 2021 Sep; 11(10):. PubMed ID: 34680056
[TBL] [Abstract][Full Text] [Related]
17. Characterization of 954 bovine full-CDS cDNA sequences.
Harhay GP; Sonstegard TS; Keele JW; Heaton MP; Clawson ML; Snelling WM; Wiedmann RT; Van Tassell CP; Smith TP
BMC Genomics; 2005 Nov; 6():166. PubMed ID: 16305752
[TBL] [Abstract][Full Text] [Related]
18. Coding DNA repeated throughout intergenic regions of the Arabidopsis thaliana genome: evolutionary footprints of RNA silencing.
Feng J; Naiman DQ; Cooper B
Mol Biosyst; 2009 Dec; 5(12):1679-87. PubMed ID: 19452047
[TBL] [Abstract][Full Text] [Related]
19. The distribution pattern of genetic variation in the transcript isoforms of the alternatively spliced protein-coding genes in the human genome.
Liu T; Lin K
Mol Biosyst; 2015 May; 11(5):1378-88. PubMed ID: 25820936
[TBL] [Abstract][Full Text] [Related]
20. Complete sequence of the maize chloroplast genome: gene content, hotspots of divergence and fine tuning of genetic information by transcript editing.
Maier RM; Neckermann K; Igloi GL; Kössel H
J Mol Biol; 1995 Sep; 251(5):614-28. PubMed ID: 7666415
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]