Unlocking hidden genomic sequence.

Abstract:

:Despite the success of conventional Sanger sequencing, significant regions of many genomes still present major obstacles to sequencing. Here we propose a novel approach with the potential to alleviate a wide range of sequencing difficulties. The technique involves extracting target DNA sequence from variants generated by introduction of random mutations. The introduction of mutations does not destroy original sequence information, but distributes it amongst multiple variants. Some of these variants lack problematic features of the target and are more amenable to conventional sequencing. The technique has been successfully demonstrated with mutation levels up to an average 18% base substitution and has been used to read previously intractable poly(A), AT-rich and GC-rich motifs.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Keith JM,Cochran DA,Lala GH,Adams P,Bryant D,Mitchelson KR

doi

10.1093/nar/gnh022

keywords:

subject

Has Abstract

pub_date

2004-02-18 00:00:00

pages

e35

issue

3

eissn

0305-1048

issn

1362-4962

pii

32/3/e35

journal_volume

32

pub_type

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