Inspecting Targeted Deep Sequencing of Whole Genome Amplified DNA Versus Fresh DNA for Somatic Mutation Detection: A Genetic Study in Myelodysplastic Syndrome Patients-Reference-Cited by-同舟云学术

Inspecting Targeted Deep Sequencing of Whole Genome Amplified DNA Versus Fresh DNA for Somatic Mutation Detection: A Genetic Study in Myelodysplastic Syndrome Patients

Published:2017-08 Issue:4 Volume:15 Page:360-365
ISSN:1947-5535
Container-title:Biopreservation and Biobanking
language:en
Short-container-title:Biopreservation and Biobanking

Author:

Palomo Laura¹,Fuster-Tormo Francisco¹,Alvira Daniel¹,Ademà Vera¹²,Armengol María Pilar³,Gómez-Marzo Paula¹,de Haro Nuri¹,Mallo Mar¹,Xicoy Blanca⁴,Zamora Lurdes⁴,Solé Francesc¹

Affiliation:

1. MDS Group, Josep Carreras Leukaemia Research Institute (IJC), ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona (Barcelona), Spain.

2. Department of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

3. Genomic and Microscopy facilities, Institut Investigació Ciències de la Salut Germans Trias i Pujol (IGTP), Badalona (Barcelona), Spain.

4. Hematology Service, ICO-Hospital Germans Trias I Pujol, Josep Carreras Leukaemia Research Institute (IJC), Universitat Autònoma De Barcelona, Badalona (Barcelona), Spain.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,General Biochemistry, Genetics and Molecular Biology,General Medicine,Medicine (miscellaneous)

Link

http://www.liebertpub.com/doi/pdf/10.1089/bio.2016.0094

Reference18 articles.

1. Unbiased Whole-Genome Amplification Directly From Clinical Samples

2. Sequencing depth and coverage: key considerations in genomic analyses

3. The role of replicates for error mitigation in next-generation sequencing

4. Single-Cell Exome Sequencing and Monoclonal Evolution of a JAK2-Negative Myeloproliferative Neoplasm

5. Exome Sequencing from Nanogram Amounts of Starting DNA: Comparing Three Approaches