Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples

Authors

Sonali P. Barwe, Alfred I. duPont Hospital for Children
Anilkumar Gopalakrisnapillai, Alfred I. duPont Hospital for Children
Nitin Mahajan, Washington University School of Medicine in St. Louis
Todd E. Druley, Washington University School of Medicine in St. Louis
E. Anders Kolb, Alfred I. duPont Hospital for Children
Erin L. Crowgey, Alfred I. duPont Hospital for Children

Journal

Genomics & Informatics

Publication Date

2020

Volume

18

Issue

1

First Page

e6

Document Type

Open Access Publication

DOI

10.5808/GI.2020.18.1.e6

Rights and Permissions

Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples. Genomics Inform. 2020;18(1):e6 Published online March 31, 2020 DOI: https://doi.org/10.5808/GI.2020.18.1.e6 CC) This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Barwe, Sonali P.; Gopalakrisnapillai, Anilkumar; Mahajan, Nitin; Druley, Todd E.; Kolb, E. Anders; and Crowgey, Erin L., "Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples." Genomics & Informatics. 18, 1. e6 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/8999