Literature DB >> 28502612

MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

Julia Wang1, Rami Al-Ouran2, Yanhui Hu3, Seon-Young Kim4, Ying-Wooi Wan5, Michael F Wangler6, Shinya Yamamoto7, Hsiao-Tuan Chao8, Aram Comjean3, Stephanie E Mohr3, Norbert Perrimon9, Zhandong Liu10, Hugo J Bellen11.   

Abstract

One major challenge encountered with interpreting human genetic variants is the limited understanding of the functional impact of genetic alterations on biological processes. Furthermore, there remains an unmet demand for an efficient survey of the wealth of information on human homologs in model organisms across numerous databases. To efficiently assess the large volume of publically available information, it is important to provide a concise summary of the most relevant information in a rapid user-friendly format. To this end, we created MARRVEL (model organism aggregated resources for rare variant exploration). MARRVEL is a publicly available website that integrates information from six human genetic databases and seven model organism databases. For any given variant or gene, MARRVEL displays information from OMIM, ExAC, ClinVar, Geno2MP, DGV, and DECIPHER. Importantly, it curates model organism-specific databases to concurrently display a concise summary regarding the human gene homologs in budding and fission yeast, worm, fly, fish, mouse, and rat on a single webpage. Experiment-based information on tissue expression, protein subcellular localization, biological process, and molecular function for the human gene and homologs in the seven model organisms are arranged into a concise output. Hence, rather than visiting multiple separate databases for variant and gene analysis, users can obtain important information by searching once through MARRVEL. Altogether, MARRVEL dramatically improves efficiency and accessibility to data collection and facilitates analysis of human genes and variants by cross-disciplinary integration of 18 million records available in public databases to facilitate clinical diagnosis and basic research.
Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ClinVar; Diopt; ExAC; FlyBase; Geno2MP; MGI; Zfin; genetic diseases; rare diseases; variants of unknown significance

Mesh:

Year:  2017        PMID: 28502612      PMCID: PMC5670038          DOI: 10.1016/j.ajhg.2017.04.010

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  44 in total

1.  Describing Sequence Variants Using HGVS Nomenclature.

Authors:  Johan T den Dunnen
Journal:  Methods Mol Biol       Date:  2017

2.  Mouse Genome Informatics (MGI): Resources for Mining Mouse Genetic, Genomic, and Biological Data in Support of Primary and Translational Research.

Authors:  Janan T Eppig; Cynthia L Smith; Judith A Blake; Martin Ringwald; James A Kadin; Joel E Richardson; Carol J Bult
Journal:  Methods Mol Biol       Date:  2017

3.  Comparison of predicted and actual consequences of missense mutations.

Authors:  Lisa A Miosge; Matthew A Field; Yovina Sontani; Vicky Cho; Simon Johnson; Anna Palkova; Bhavani Balakishnan; Rong Liang; Yafei Zhang; Stephen Lyon; Bruce Beutler; Belinda Whittle; Edward M Bertram; Anselm Enders; Christopher C Goodnow; T Daniel Andrews
Journal:  Proc Natl Acad Sci U S A       Date:  2015-08-12       Impact factor: 11.205

4.  Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.

Authors:  Ender Karaca; Tamar Harel; Davut Pehlivan; Shalini N Jhangiani; Tomasz Gambin; Zeynep Coban Akdemir; Claudia Gonzaga-Jauregui; Serkan Erdin; Yavuz Bayram; Ian M Campbell; Jill V Hunter; Mehmed M Atik; Hilde Van Esch; Bo Yuan; Wojciech Wiszniewski; Sedat Isikay; Gozde Yesil; Ozge O Yuregir; Sevcan Tug Bozdogan; Huseyin Aslan; Hatip Aydin; Tulay Tos; Ayse Aksoy; Darryl C De Vivo; Preti Jain; B Bilge Geckinli; Ozlem Sezer; Davut Gul; Burak Durmaz; Ozgur Cogulu; Ferda Ozkinay; Vehap Topcu; Sukru Candan; Alper Han Cebi; Mevlit Ikbal; Elif Yilmaz Gulec; Alper Gezdirici; Erkan Koparir; Fatma Ekici; Salih Coskun; Salih Cicek; Kadri Karaer; Asuman Koparir; Mehmet Bugrahan Duz; Emre Kirat; Elif Fenercioglu; Hakan Ulucan; Mehmet Seven; Tulay Guran; Nursel Elcioglu; Mahmut Selman Yildirim; Dilek Aktas; Mehmet Alikaşifoğlu; Mehmet Ture; Tahsin Yakut; John D Overton; Adnan Yuksel; Mustafa Ozen; Donna M Muzny; David R Adams; Eric Boerwinkle; Wendy K Chung; Richard A Gibbs; James R Lupski
Journal:  Neuron       Date:  2015-11-04       Impact factor: 17.173

5.  The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine.

Authors:  William A Gahl; John J Mulvihill; Camilo Toro; Thomas C Markello; Anastasia L Wise; Rachel B Ramoni; David R Adams; Cynthia J Tifft
Journal:  Mol Genet Metab       Date:  2016-01-22       Impact factor: 4.797

6.  Loss of Nardilysin, a Mitochondrial Co-chaperone for α-Ketoglutarate Dehydrogenase, Promotes mTORC1 Activation and Neurodegeneration.

Authors:  Wan Hee Yoon; Hector Sandoval; Sonal Nagarkar-Jaiswal; Manish Jaiswal; Shinya Yamamoto; Nele A Haelterman; Nagireddy Putluri; Vasanta Putluri; Arun Sreekumar; Tulay Tos; Ayse Aksoy; Taraka Donti; Brett H Graham; Mikiko Ohno; Eiichiro Nishi; Jill Hunter; Donna M Muzny; Jason Carmichael; Joseph Shen; Valerie A Arboleda; Stanley F Nelson; Michael F Wangler; Ender Karaca; James R Lupski; Hugo J Bellen
Journal:  Neuron       Date:  2016-12-22       Impact factor: 17.173

Review 7.  Single nucleotide variations: biological impact and theoretical interpretation.

Authors:  Panagiotis Katsonis; Amanda Koire; Stephen Joseph Wilson; Teng-Kuei Hsu; Rhonald C Lua; Angela Dawn Wilkins; Olivier Lichtarge
Journal:  Protein Sci       Date:  2014-10-20       Impact factor: 6.725

8.  The Rat Genome Database 2015: genomic, phenotypic and environmental variations and disease.

Authors:  Mary Shimoyama; Jeff De Pons; G Thomas Hayman; Stanley J F Laulederkind; Weisong Liu; Rajni Nigam; Victoria Petri; Jennifer R Smith; Marek Tutaj; Shur-Jen Wang; Elizabeth Worthey; Melinda Dwinell; Howard Jacob
Journal:  Nucleic Acids Res       Date:  2014-10-29       Impact factor: 19.160

9.  Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Authors:  Brian J O'Roak; Pelagia Deriziotis; Choli Lee; Laura Vives; Jerrod J Schwartz; Santhosh Girirajan; Emre Karakoc; Alexandra P Mackenzie; Sarah B Ng; Carl Baker; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Simon E Fisher; Jay Shendure; Evan E Eichler
Journal:  Nat Genet       Date:  2011-05-15       Impact factor: 38.330

10.  WormBase 2016: expanding to enable helminth genomic research.

Authors:  Kevin L Howe; Bruce J Bolt; Scott Cain; Juancarlos Chan; Wen J Chen; Paul Davis; James Done; Thomas Down; Sibyl Gao; Christian Grove; Todd W Harris; Ranjana Kishore; Raymond Lee; Jane Lomax; Yuling Li; Hans-Michael Muller; Cecilia Nakamura; Paulo Nuin; Michael Paulini; Daniela Raciti; Gary Schindelman; Eleanor Stanley; Mary Ann Tuli; Kimberly Van Auken; Daniel Wang; Xiaodong Wang; Gary Williams; Adam Wright; Karen Yook; Matthew Berriman; Paul Kersey; Tim Schedl; Lincoln Stein; Paul W Sternberg
Journal:  Nucleic Acids Res       Date:  2015-11-17       Impact factor: 16.971

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  83 in total

1.  De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment.

Authors:  Debdeep Dutta; Lauren C Briere; Oguz Kanca; Paul C Marcogliese; Melissa A Walker; Frances A High; Adeline Vanderver; Joel Krier; Nikkola Carmichael; Christine Callahan; Ryan J Taft; Cas Simons; Guy Helman; Undiagnosed Diseases Network; Michael F Wangler; Shinya Yamamoto; David A Sweetser; Hugo J Bellen
Journal:  Hum Mol Genet       Date:  2020-06-03       Impact factor: 6.150

Review 2.  High-throughput mouse phenomics for characterizing mammalian gene function.

Authors:  Steve D M Brown; Chris C Holmes; Ann-Marie Mallon; Terrence F Meehan; Damian Smedley; Sara Wells
Journal:  Nat Rev Genet       Date:  2018-06       Impact factor: 53.242

Review 3.  Measuring intolerance to mutation in human genetics.

Authors:  Zachary L Fuller; Jeremy J Berg; Hakhamanesh Mostafavi; Guy Sella; Molly Przeworski
Journal:  Nat Genet       Date:  2019-04-08       Impact factor: 38.330

4.  MendelVar: gene prioritisation at GWAS loci using phenotypic enrichment of mendelian disease genes.

Authors:  Sobczyk M K; Gaunt T R; Paternoster L
Journal:  Bioinformatics       Date:  2021-01-16       Impact factor: 6.937

5.  Model matchmaking.

Authors:  Ellen P Neff
Journal:  Lab Anim (NY)       Date:  2021-02       Impact factor: 12.625

Review 6.  Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing.

Authors:  Abdul Rezzak Hamzeh; T Daniel Andrews; Matt A Field
Journal:  Methods Mol Biol       Date:  2021

Review 7.  Model organism data evolving in support of translational medicine.

Authors:  Douglas G Howe; Judith A Blake; Yvonne M Bradford; Carol J Bult; Brian R Calvi; Stacia R Engel; James A Kadin; Thomas C Kaufman; Ranjana Kishore; Stanley J F Laulederkind; Suzanna E Lewis; Sierra A T Moxon; Joel E Richardson; Cynthia Smith
Journal:  Lab Anim (NY)       Date:  2018-09-17       Impact factor: 12.625

8.  Heritability of Regional Brain Volumes in Large-Scale Neuroimaging and Genetic Studies.

Authors:  Bingxin Zhao; Joseph G Ibrahim; Yun Li; Tengfei Li; Yue Wang; Yue Shan; Ziliang Zhu; Fan Zhou; Jingwen Zhang; Chao Huang; Huiling Liao; Liuqing Yang; Paul M Thompson; Hongtu Zhu
Journal:  Cereb Cortex       Date:  2019-07-05       Impact factor: 5.357

Review 9.  Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases.

Authors:  Jose L Salazar; Shinya Yamamoto
Journal:  Adv Exp Med Biol       Date:  2018       Impact factor: 2.622

10.  Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.

Authors:  Ning Liu; Kelly Schoch; Xi Luo; Loren D M Pena; Venkata Hemanjani Bhavana; Mary K Kukolich; Sarah Stringer; Zöe Powis; Kelly Radtke; Cameron Mroske; Kristen L Deak; Marie T McDonald; Allyn McConkie-Rosell; M Louise Markert; Peter G Kranz; Nicholas Stong; Anna C Need; David Bick; Michelle D Amaral; Elizabeth A Worthey; Shawn Levy; Michael F Wangler; Hugo J Bellen; Vandana Shashi; Shinya Yamamoto
Journal:  Hum Mol Genet       Date:  2018-07-15       Impact factor: 6.150

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