Next-Generation Sequencing technologies (NGS) are trasforming today's biology by making it economically feasible to read the complete genome of individuals. Single nucleotide polymorphism (SNP) is the most common form of individual DNA variation; and the set of SNPs present in a chromosome (called the haplotype) is of interest in a wide area of applications in molecular biology and biomedicine. Personalized haplotyping of (portions of/all) the chromosomes of individuals through NGS is one of themost promising basic ingredients leading

ReHap: A framework for single individual haplotyping from next-generation sequencing data

Geraci F;Pellegrini M
2011

Abstract

Next-Generation Sequencing technologies (NGS) are trasforming today's biology by making it economically feasible to read the complete genome of individuals. Single nucleotide polymorphism (SNP) is the most common form of individual DNA variation; and the set of SNPs present in a chromosome (called the haplotype) is of interest in a wide area of applications in molecular biology and biomedicine. Personalized haplotyping of (portions of/all) the chromosomes of individuals through NGS is one of themost promising basic ingredients leading
2011
Istituto di informatica e telematica - IIT
Inglese
Biomedical Engineering Systems and Technologies
322
333
12
978-3-642-18471-0
http://www.scopus.com/inward/record.url?eid=2-s2.0-79952529634&partnerID=q2rCbXpz
Sì, ma tipo non specificato
bionformatica
2
02 Contributo in Volume::02.01 Contributo in volume (Capitolo o Saggio)
268
none
Geraci, F; Pellegrini, M
info:eu-repo/semantics/bookPart
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/314799
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