CrossRef Text and Data Mining
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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
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   Crossref logo
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High concordance between next generation sequencing and single-nucleotide polymorphism array in preimplantation genetic testing for aneuploid
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Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling
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A review of somatic single nucleotide variant calling algorithms for next-generation sequencing data
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Analysis of Structural Chromosome Variants by Next Generation Sequencing Methods
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Single Nucleotide Variant Detection Using Next Generation Sequencing
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Primary renal NUT carcinoma identified by next-generation sequencing: A case report and literature review
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Genome Editing as a Tool toward Better Functional Understanding of Variants Identified by Next-Generation Sequencing
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Functional validation of genetic variants identified by next generation sequencing in malformations of cortical development
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Accurate detection of subclonal variants in paired diagnosis-relapse acute myeloid leukemia samples by next generation Duplex Sequencing
Leukemia Research. 2022;115:106822   Crossref logo
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