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Simple sequence repeat variations expedite phage divergence: Mechanisms of indels and gene mutations
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 2016Phages are the most abundant biological entities and influence prokaryotic communities on Earth. Comparing closely related genomes sheds light on molecular events shaping phage evolution. Simple sequence repeat (SSR) variations impart over half of the genomic changes between T7M and T3, indicating an important role of SSRs in accelerating phage genetic
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[A novel indel NF1 mutation identified in a patient with neurofibromatosis type 1].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2015To identify the genetic etiology in a Chinese patient with neurofibromatosis type 1 (NF-1).All coding exons and the flanking sequences of neurofibromin 1 (NF1) gene from the patient were captured, individually barcoded and subjected to HiSeq2000 high-throughput sequencing.
Tieshan, Zhu +4 more
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A universal SNP and small-indel variant caller using deep neural networks
Nature Biotechnology, 2018Ryan Poplin +2 more
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Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
Nature Biotechnology, 2014Justin M Zook +2 more
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Digital Droplet Polymerase Chain Reaction for Indel Mutation Detection in Target Genes
Journal of Visualized Experiments, 2023openaire +2 more sources
ABRA: improved coding indel detection via assembly-based realignment
Bioinformatics, 2014Matthew D Wilkerson +2 more
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p53 inhibits CRISPR–Cas9 engineering in human pluripotent stem cells
Nature Medicine, 2018Chaoyang Ye +2 more
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