Cargando…

VarI-SIG 2014 - From SNPs to variants: interpreting different types of genetic variants

Detalles Bibliográficos
Autores principales:	Bromberg, Yana, Capriotti, Emidio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Introduction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480323/ https://www.ncbi.nlm.nih.gov/pubmed/26110281 http://dx.doi.org/10.1186/1471-2164-16-S8-I1

Ejemplares similares

VarI-COSI 2018: a forum for research advances in variant interpretation and diagnostics
por: Bromberg, Yana, et al.
Publicado: (2019)

SNP-SIG 2013: from coding to non-coding - new approaches for genomic variant interpretation
por: Bromberg, Yana, et al.
Publicado: (2014)

SNP-SIG Meeting 2011: Identification and annotation of SNPs in the context of structure, function, and disease
por: Bromberg, Yana, et al.
Publicado: (2012)

VarI-SIG 2015: methods for personalized medicine – the role of variant interpretation in research and diagnostics
por: Bromberg, Yana, et al.
Publicado: (2016)

Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations
por: Bromberg, Yana, et al.
Publicado: (2013)

Collective judgment predicts disease-associated single nucleotide variants
por: Capriotti, Emidio, et al.
Publicado: (2013)

Integrating molecular networks with genetic variant interpretation for precision medicine
por: Capriotti, Emidio, et al.
Publicado: (2018)

FEPI-MB: identifying SNPs-disease association using a Markov Blanket-based approach
por: Han, Bing, et al.
Publicado: (2011)

Computational methods and resources for the interpretation of genomic variants in cancer
por: Tian, Rui, et al.
Publicado: (2015)

London Trauma Conference 2014
por: Salm, Leopold, et al.
Publicado: (2015)

TraPS-VarI: Identifying genetic variants altering phosphotyrosine based signalling motifs
por: Ulaganathan, Vijay Kumar
Publicado: (2020)

Between proteins and phenotypes: annotation and interpretation of mutations
por: Baker, Christopher JO, et al.
Publicado: (2009)

Connecting the dots in translational bioinformatics: TBC 2014 collection
por: Kim, Ju Han
Publicado: (2015)

Analysis and Interpretation of the Impact of Missense Variants in Cancer
por: Petrosino, Maria, et al.
Publicado: (2021)

Preface: BITS2014, the annual meeting of the Italian Society of Bioinformatics
por: Facchiano, Angelo, et al.
Publicado: (2015)

Highlights from the tenth ISCB Student Council Symposium 2014
por: Rahman, Farzana, et al.
Publicado: (2015)

InCoB2014: bioinformatics to tackle the data to knowledge challenge
por: Ranganathan, Shoba, et al.
Publicado: (2014)

Advancing reproductive health on the humanitarian agenda: the 2012-2014 global review
por: Chynoweth, Sarah K
Publicado: (2015)

Proceedings of the 2014 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference
por: Wren, Jonathan D, et al.
Publicado: (2014)

InCoB2014: Systems Biology update from the Asia-Pacific
por: Ranganathan, Shoba, et al.
Publicado: (2014)

Advances in emergency medicine research in India: abstracts from the EMCON 2014 international conference
por: Kapur, Bobby, et al.
Publicado: (2015)

Highlights from the 1st ISCB Latin American Student Council Symposium 2014
por: Parra, R Gonzalo, et al.
Publicado: (2015)

New trends in biomedical engineering and bioinformatics applied to biomedicine - special issue of IWBBIO 2014
por: Ortuño, Franscisco M, et al.
Publicado: (2015)

InCoB2014: mining biological data from genomics for transforming industry and health
por: Schönbach, Christian, et al.
Publicado: (2014)

Clinical Laboratories Collaborate to Resolve Differences in Variant Interpretations Submitted to ClinVar
por: Harrison, Steven M., et al.
Publicado: (2017)

iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification
por: Castellano, Sara, et al.
Publicado: (2021)

ClinVar: public archive of interpretations of clinically relevant variants
por: Landrum, Melissa J., et al.
Publicado: (2016)

ClinVar: improving access to variant interpretations and supporting evidence
por: Landrum, Melissa J, et al.
Publicado: (2018)

ClinVar Is a Critical Resource to Advance Variant Interpretation
por: Rehm, Heidi L., et al.
Publicado: (2017)

WS-SNPs&GO: a web server for predicting the deleterious effect of human protein variants using functional annotation
por: Capriotti, Emidio, et al.
Publicado: (2013)

Genetics research at the "Centenary of human population genetics" conference and SBB-2019
por: Tatarinova, Tatiana V., et al.
Publicado: (2020)

In-silico Analysis of NF1 Missense Variants in ClinVar: Translating Variant Predictions into Variant Interpretation and Classification
por: Accetturo, Matteo, et al.
Publicado: (2020)

iDASH secure genome analysis competition 2017
por: Wang, XiaoFeng, et al.
Publicado: (2018)

Computational models in genetics at BGRS-2018
por: Orlov, Yuriy L., et al.
Publicado: (2019)

Editorial: Mathematical problems in physical fluid dynamics: part I
por: Goluskin, D., et al.
Publicado: (2022)

Time-keeping and decision-making in living cells: Part I
por: Tyson, John J., et al.
Publicado: (2022)

Genetics at Belyaev Conference – 2017: introductory note
por: Orlov, Yuriy L., et al.
Publicado: (2017)

Medical genetics studies at BGRS conference series
por: Baranova, Ancha V., et al.
Publicado: (2019)

Diversity, population genetics, and phylogeography of selected wild mushrooms
por: Xu, Jianping, et al.
Publicado: (2015)

Introduction: the secret lives of microbial mobile genetic elements
por: Hall, James P. J., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_16m9h206j9919njm7rk2ao2kgb