Deep sequencing data analysis

DOI10.1007/978-1-0716-1103-6MaRDI QIDQ2034478zbMATH OpenOpenAlexFDO

Authors

Publication date 22 June 2021

Published in Methods in Molecular Biology (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1007/978-1-0716-1103-6

zbMATH Keywords

16S amplicon sequencingATACseqcancer classificationcausal variantschromatin landscapeclonal evolutioncommunity detection algorithmscopy number variationde novo mutationsdeep learningdeep sequencingforensic analysisimputation of untyped variantsintra-tumour heterogeneityMendelian disordermicrobiome sequencingmulti-region sequence analysisnon-invasive prenatal diagnosisRNA-seq experimental designsingle cell microRNA analysissingle cell transcriptome profilingsingle nucleotide polymorphism (SNP)small universal k-mer hitting setwhole-metagenome shotgun sequencing

Mathematics Subject Classification ID

Collections of articles of miscellaneous specific interest (00B15) Proceedings, conferences, collections, etc. pertaining to biology (92-06) Genetics and epigenetics (92D10) Protein sequences, DNA sequences (92D20)

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Cited in

(5)

• Statistical analysis of next generation sequencing data
• Next-generation sequencing. Current technologies and applications
• Computational genomics with R. With the assistance of Verdan Franke, Bora Uyar and Jonathan Ronen
• Computational exome and genome analysis
• Genome sequencing technology and algorithms.

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