ID

45569

Descripción

Principal Investigator: Stacey Gabriel, The Broad Institute, Boston, MA, USA MeSH: Muscular Dystrophies,Myopathies, Structural, Congenital,Arthrogryposis https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000655 The samples are drawn from a collection of patients with a heterogeneous set of neuromuscular disorders, including congenital muscular dystrophy, congenital myopathy, limb-girdle muscular dystrophy, Emery-Dreifuss muscular dystrophy, and arthrogryposis, along with unaffected parents and siblings in some cases. The samples were collected by the following clinicians affiliated with the associated institutes:- Kathryn North and Nigel Clarke (Institute for Neuroscience and Muscle Research, Children's Hospital at Westmead, Australia) - Hanns Lochmuller and Kate Bushby (The Newcastle Muscle Centre, Newcastle University, UK) - Peter Kang (Boston Children's Hospital) - Carsten Bonnemann (National Institutes of Health, Bethesda, MD, USA) - Nigel Laing (University of Western Australia) All exome sequencing was performed at the Broad Institute of Harvard and MIT; samples sequence capture was performed using Agilent SureSelect Human All Exon Kit v2 or Illumina's Rapid Capture Exome enrichment kit and sequencing was performed on an Illumina HiSeq 2000. In addition some samples were whole genome sequenced on Illumina HiSeq X Ten.

Link

dbGaP study = phs000655

Palabras clave

Versiones (1)

1. 23/1/23 23/1/23 - Dr. Christian Niklas

Titular de derechos de autor

Stacey Gabriel, The Broad Institute, Boston, MA, USA

Subido en

23 de enero de 2023

DOI

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