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| Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples |
| Sonali P. Barwe, Anilkumar Gopalakrisnapillai, Nitin Mahajan, Todd E. Druley, E. Anders Kolb, Erin L. Crowgey |
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Genomics Inform. 2020;18(1):e6 Published online March 31, 2020 DOI: https://doi.org/10.5808/GI.2020.18.1.e6 |
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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. 2020;18(1):e6  High concordance between next generation sequencing and single-nucleotide polymorphism array in preimplantation genetic testing for aneuploid . 2020; Concordance between single-nucleotide polymorphism–based genomic instability assays and a next-generation sequencing–based homologous recombination deficiency test BMC Cancer. 2022;22(1): Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling The Plant Journal. 2011;67(4):736-745 A PEDIATRIC BURKITT LYMPHOMA PATIENT-DERIVED XENOGRAFT RESOURCE OF PRIMARY AND RELAPSE/REFRACTORY DISEASE Leukemia Research. 2022;121:S48-S49 A review of somatic single nucleotide variant calling algorithms for next-generation sequencing data Computational and Structural Biotechnology Journal. 2018;16:15-24 Analysis of Structural Chromosome Variants by Next Generation Sequencing Methods Clinical Applications for Next-Generation Sequencing. 2016;39-61 Single Nucleotide Variant Detection Using Next Generation Sequencing Clinical Genomics. 2015;109-127 Primary renal NUT carcinoma identified by next-generation sequencing: A case report and literature review . 2020; Genome Editing as a Tool toward Better Functional Understanding of Variants Identified by Next-Generation Sequencing Clinical Chemistry. 2015;61(3):564-565 |
