Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer

Roberta Bordoni, Raoul Bonnal, Ermanno Rizzi, Paola Carrera, Sara Benedetti, Laura Cremonesi, Stefania Stenirri, Alessio Colombo, Cristina Montrasio, Sara Bonalumi, Alberto Albertini, Luigi Bernardi, Maurizio Ferrari, Gianluca De Bellis

Research output: Contribution to journalArticlepeer-review

Abstract

Background: A new priority in genome research is large-scale resequencing of genes to understand the molecular basis of hereditary disease and cancer. We assessed the ability of massively parallel pyrosequencing to identify sequence variants in pools. From a large collection of human PCR samples we selected 343 PCR products belonging to 16 disease genes and including a large spectrum of sequence variations previously identified by Sanger sequencing. The sequence variants included SNPs and small deletions and insertions (up to 44 bp), in homozygous or heterozygous state. Results: The DNA was combined in 4 pools containing from 27 to 164 amplicons and from 8,9 to 50,8 Kb to sequence for a total of 110 Kb. Pyrosequencing generated over 80 million base pairs of data. Blind searching for sequence variations with a specifically designed bioinformatics procedure identified 465 putative sequence variants, including 412 true variants, 53 false positives (in or adjacent to homopolymeric tracts), no false negatives. All known variants in positions covered with at least 30× depth were correctly recognized. Conclusion: Massively parallel pyrosequencing may be used to simplify and speed the search for DNA variations in PCR products. Our results encourage further studies to evaluate molecular diagnostics applications.

Original languageEnglish
Article number464
JournalBMC Genomics
Volume9
DOIs
Publication statusPublished - Oct 8 2008

ASJC Scopus subject areas

  • Biotechnology
  • Genetics

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