» Articles » PMID: 30486838

CHESS: a New Human Gene Catalog Curated from Thousands of Large-scale RNA Sequencing Experiments Reveals Extensive Transcriptional Noise

Overview
Journal Genome Biol
Specialties Biology
Genetics
Date 2018 Nov 30
PMID 30486838
Citations 159
Authors
Affiliations
Soon will be listed here.
Abstract

We assembled the sequences from deep RNA sequencing experiments by the Genotype-Tissue Expression (GTEx) project, to create a new catalog of human genes and transcripts, called CHESS. The new database contains 42,611 genes, of which 20,352 are potentially protein-coding and 22,259 are noncoding, and a total of 323,258 transcripts. These include 224 novel protein-coding genes and 116,156 novel transcripts. We detected over 30 million additional transcripts at more than 650,000 genomic loci, nearly all of which are likely nonfunctional, revealing a heretofore unappreciated amount of transcriptional noise in human cells. The CHESS database is available at http://ccb.jhu.edu/chess .

Citing Articles

Accurate transcription unit annotation from run-on and sequencing data.

Munn P, Chia J, Danko C bioRxiv. 2025; .

PMID: 40027686 PMC: 11870431. DOI: 10.1101/2025.02.12.637853.


5'-UTR G-Quadruplex-Mediated Translation Regulation in Eukaryotes: Current Understanding and Methodological Challenges.

Kamzeeva P, Alferova V, Korshun V, Varizhuk A, Aralov A Int J Mol Sci. 2025; 26(3).

PMID: 39940956 PMC: 11818886. DOI: 10.3390/ijms26031187.


Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.

Qu H, Delfiner M, Gangireddy C, Vaidya A, Nguyen K, Whitman I J Mol Med (Berl). 2024; 103(2):175-185.

PMID: 39730912 PMC: 11799050. DOI: 10.1007/s00109-024-02510-z.


Human introns contain conserved tissue-specific cryptic poison exons.

Margasyuk S, Kuznetsova A, Zavileyskiy L, Vlasenok M, Skvortsov D, Pervouchine D NAR Genom Bioinform. 2024; 6(4):lqae163.

PMID: 39664813 PMC: 11632617. DOI: 10.1093/nargab/lqae163.


Translation of circular RNAs.

Margvelani G, Maquera K, Welden J, Rodgers D, Stamm S Nucleic Acids Res. 2024; 53(1.

PMID: 39660652 PMC: 11724312. DOI: 10.1093/nar/gkae1167.


References
1.
Pertea M, Kim D, Pertea G, Leek J, Salzberg S . Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown. Nat Protoc. 2016; 11(9):1650-67. PMC: 5032908. DOI: 10.1038/nprot.2016.095. View

2.
Antequera F, Bird A . Predicting the total number of human genes. Nat Genet. 1994; 8(2):114. DOI: 10.1038/ng1094-114a. View

3.
Chen Y, Iseli C, Venditti C, Old L, Simpson A, Jongeneel C . Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome. Genes Chromosomes Cancer. 2005; 45(4):392-400. DOI: 10.1002/gcc.20298. View

4.
Need A, Shashi V, Hitomi Y, Schoch K, Shianna K, McDonald M . Clinical application of exome sequencing in undiagnosed genetic conditions. J Med Genet. 2012; 49(6):353-61. PMC: 3375064. DOI: 10.1136/jmedgenet-2012-100819. View

5.
Zhu X, Petrovski S, Xie P, Ruzzo E, Lu Y, McSweeney K . Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genet Med. 2015; 17(10):774-81. PMC: 4791490. DOI: 10.1038/gim.2014.191. View