Literature DB >> 30977936

A snapshot of some pLI score pitfalls.

Alban Ziegler1, Estelle Colin1,2, David Goudenège2, Dominique Bonneau1,2.   

Abstract

The pLI score reflects the tolerance of a given gene to the loss of function on the basis of the number of protein truncating variants, that is, the frameshift, splice donor, splice acceptor, and stop-gain variants referenced for this gene in control databases weighted by the size of the gene and the sequencing coverage. It is frequently used to prioritize candidate genes when analyzing whole exome or whole genome data. We list here the main pitfalls to consider before using this score. Concrete illustrations are given for each of these pitfalls.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  exome sequencing analysis; loss of function; pLI score

Mesh:

Substances:

Year:  2019        PMID: 30977936     DOI: 10.1002/humu.23763

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  11 in total

1.  An overview of germline variations in genes of primary immunodeficiences through integrative analysis of ClinVar, HGMD® and dbSNP databases.

Authors:  Lyubov E Salnikova; Dmitry S Kolobkov; Darya A Sviridova; Serikbai K Abilev
Journal:  Hum Genet       Date:  2021-07-16       Impact factor: 4.132

2.  Dietary modification, penetrance, and the origins of congenital malformation.

Authors:  Greg Gibson; Kiera Berger
Journal:  Proc Natl Acad Sci U S A       Date:  2020-02-18       Impact factor: 11.205

3.  No preferential mode of inheritance for highly constrained genes.

Authors:  Alexandre Fabre; Julien Mancini
Journal:  Intractable Rare Dis Res       Date:  2022-02

4.  A Novel Variant of X-Linked Moesin Gene in a Boy With Inflammatory Bowel Disease Like Disease-A Case Report.

Authors:  Youhong Fang; Youyou Luo; Yang Liu; Jie Chen
Journal:  Front Genet       Date:  2022-06-09       Impact factor: 4.772

5.  The 3D mutational constraint on amino acid sites in the human proteome.

Authors:  Bian Li; Dan M Roden; John A Capra
Journal:  Nat Commun       Date:  2022-06-07       Impact factor: 17.694

6.  Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles.

Authors:  Lubica Dudakova; Viktor Stranecky; Lenka Piherova; Tomas Palecek; Nikolas Pontikos; Stanislav Kmoch; Pavlina Skalicka; Manuela Vaneckova; Alice E Davidson; Petra Liskova
Journal:  Genes (Basel)       Date:  2021-04-30       Impact factor: 4.096

7.  Unified inference of missense variant effects and gene constraints in the human genome.

Authors:  Yi-Fei Huang
Journal:  PLoS Genet       Date:  2020-07-15       Impact factor: 5.917

Review 8.  Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy.

Authors:  Gabrielle Wheway; Andrew Douglas; Diana Baralle; Elsa Guillot
Journal:  Exp Eye Res       Date:  2020-01-31       Impact factor: 3.467

9.  Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.

Authors:  Polakit Teekakirikul; Wenjuan Zhu; George C Gabriel; Cullen B Young; Kylia Williams; Lisa J Martin; Jennifer C Hill; Tara Richards; Marie Billaud; Julie A Phillippi; Jianbin Wang; Yijen Wu; Tuantuan Tan; William Devine; Jiuann-Huey Lin; Abha S Bais; Jonathan Klonowski; Anne Moreau de Bellaing; Ankur Saini; Michael X Wang; Leonid Emerel; Nathan Salamacha; Samuel K Wyman; Carrie Lee; Hung Sing Li; Anastasia Miron; Jingyu Zhang; Jianhua Xing; Dennis M McNamara; Erik Fung; Paul Kirshbom; William Mahle; Lazaros K Kochilas; Yihua He; Vidu Garg; Peter White; Kim L McBride; D Woodrow Benson; Thomas G Gleason; Seema Mital; Cecilia W Lo
Journal:  HGG Adv       Date:  2021-07-29

Review 10.  Mutations in Hsp90 Cochaperones Result in a Wide Variety of Human Disorders.

Authors:  Jill L Johnson
Journal:  Front Mol Biosci       Date:  2021-12-08
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