Targeted resequencing of the EGFR and MET genes using the Fluidigm Access Array System and the Roche GS Junior System

Clotilde Teiling; Ben Boese; Martin Pieprzyk

doi:10.2144/000113740

Targeted resequencing of the EGFR and MET genes using the Fluidigm Access Array System and the Roche GS Junior System

BioTechniques ◽

10.2144/000113740 ◽

2011 ◽

Vol 51 (3) ◽

Cited By ~ 1

Author(s):

Clotilde Teiling ◽

Ben Boese ◽

Martin Pieprzyk

Keyword(s):

Targeted Resequencing ◽

Fluidigm Access Array

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Faculty Opinions recommendation of Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.718016749.793477893 ◽

2013 ◽

Author(s):

Bert de Vries

Keyword(s):

De Novo ◽

De Novo Mutations ◽

Epileptic Encephalopathies ◽

Targeted Resequencing

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Faculty Opinions recommendation of Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.736138350.793562386 ◽

2019 ◽

Author(s):

Fowzan S Alkuraya

Keyword(s):

Pathogenic Variant ◽

Erythropoietic Protoporphyria ◽

Targeted Resequencing ◽

Dependent Mechanism

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Targeted Resequencing and Analysis of the Diamond-Blackfan Anemia Disease Locus RPS19

PLoS ONE ◽

10.1371/journal.pone.0006172 ◽

2009 ◽

Vol 4 (7) ◽

pp. e6172 ◽

Cited By ~ 9

Author(s):

Alvaro Martinez Barrio ◽

Oskar Eriksson ◽

Jitendra Badhai ◽

Anne-Sophie Fröjmark ◽

Erik Bongcam-Rudloff ◽

...

Keyword(s):

Disease Locus ◽

Targeted Resequencing ◽

Diamond Blackfan Anemia

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Overlapping pools for high-throughput targeted resequencing

Genome Research ◽

10.1101/gr.088559.108 ◽

2009 ◽

Vol 19 (7) ◽

pp. 1254-1261 ◽

Cited By ~ 53

Author(s):

S. Prabhu ◽

I. Pe'er

Keyword(s):

High Throughput ◽

Targeted Resequencing

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Targeted Resequencing and Systematic In Vivo Functional Testing Identifies Rare Variants in MEIS1 as Significant Contributors to Restless Legs Syndrome

The American Journal of Human Genetics ◽

10.1016/j.ajhg.2014.06.005 ◽

2014 ◽

Vol 95 (1) ◽

pp. 85-95 ◽

Cited By ~ 35

Author(s):

Eva C. Schulte ◽

Maria Kousi ◽

Perciliz L. Tan ◽

Erik Tilch ◽

Franziska Knauf ◽

...

Keyword(s):

Restless Legs Syndrome ◽

Rare Variants ◽

Functional Testing ◽

Targeted Resequencing ◽

Restless Legs

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Identification of Causal and/or Rare Genetic Variants for Complex Traits by Targeted Resequencing in Population-based Cohorts

Genomics & Informatics ◽

10.5808/gi.2010.8.3.131 ◽

2010 ◽

Vol 8 (3) ◽

pp. 131-137 ◽

Cited By ~ 1

Author(s):

Yun-Kyoung Kim ◽

Chang-Bum Hong ◽

Yoon-Shin Cho

Keyword(s):

Genetic Variants ◽

Complex Traits ◽

Population Based ◽

Targeted Resequencing ◽

Rare Genetic Variants

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Targeted resequencing reveals genetic risks in patients with sporadic idiopathic pulmonary fibrosis

Human Mutation ◽

10.1002/humu.23566 ◽

2018 ◽

Vol 39 (9) ◽

pp. 1238-1245 ◽

Cited By ~ 13

Author(s):

Yanhan Deng ◽

Zongzhe Li ◽

Juan Liu ◽

Zheng Wang ◽

Yanyan Cao ◽

...

Keyword(s):

Idiopathic Pulmonary Fibrosis ◽

Pulmonary Fibrosis ◽

Targeted Resequencing ◽

Genetic Risks

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Targeted resequencing of coding DNA sequences for SNP discovery in nonmodel species

Molecular Ecology Resources ◽

10.1111/1755-0998.12924 ◽

2018 ◽

Vol 18 (6) ◽

pp. 1356-1373 ◽

Cited By ~ 7

Author(s):

Daniel W. Förster ◽

James K. Bull ◽

Dorina Lenz ◽

Marijke Autenrieth ◽

Johanna L. A. Paijmans ◽

...

Keyword(s):

Dna Sequences ◽

Snp Discovery ◽

Targeted Resequencing

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Targeted resequencing identifiesPTCH1as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network

Genome Research ◽

10.1101/gr.196048.115 ◽

2016 ◽

Vol 26 (4) ◽

pp. 474-485 ◽

Cited By ~ 22

Author(s):

Nicolas Chassaing ◽

Erica E. Davis ◽

Kelly L. McKnight ◽

Adrienne R. Niederriter ◽

Alexandre Causse ◽

...

Keyword(s):

Regulatory Network ◽

Major Contributor ◽

Developmental Anomalies ◽

Targeted Resequencing

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Targeted resequencing of FECH locus reveals that a novel deep intronic pathogenic variant and eQTLs may cause erythropoietic protoporphyria (EPP) through a methylation-dependent mechanism

Genetics in Medicine ◽

10.1038/s41436-019-0584-0 ◽

2019 ◽

Vol 22 (1) ◽

pp. 35-43 ◽

Cited By ~ 2

Author(s):

Matteo Chiara ◽

Ilaria Primon ◽

Letizia Tarantini ◽

Luca Agnelli ◽

Valentina Brancaleoni ◽

...

Keyword(s):

Pathogenic Variant ◽

Erythropoietic Protoporphyria ◽

Targeted Resequencing ◽

Dependent Mechanism

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