Indel variant analysis of short-read sequencing data with Scalpel - Fang, Han; Bergmann, Ewa A; Arora, Kanika; Vacic, Vladimir; Zody, Michael C; Iossifov, Ivan; O'Rawe, Jason A; Wu, Yiyang; Jimenez Barron, Laura T; Rosenbaum, Julie; Ronemus, Michael; Lee, Yoon-ha; et al. (Nature protocols, 2016)
Keywords: 13/100; 13/31; 14/63; 631/114/2785; 631/1647/794; 631/208/212; 631/208/514/2254; 631/208/726/649; Algorithms; Alleles; Analytical Chemistry; Annotations; Autism; Biological Techniques; Computational Biology/Bioinformatics; Computer applications; DNA Mutational Analysis - methods; DNA sequencing; Gene mapping; Gene mutation; Gene sequencing; Genetic variation; Genomes; Genomics; High-Throughput Nucleotide Sequencing - methods; Humans; Identification and classification; INDEL Mutation; Life Sciences; Methods; Microarrays; Molecular Sequence Annotation; Mutation; Organic Chemistry; Polymorphism, Single Nucleotide; protocol; Source code; New York; United States--US