Literature DB >> 10424466

An estimate of the crosstalk matrix in four-dye fluorescence-based DNA sequencing.

L Li1, T P Speed.   

Abstract

Color separation is an essential step of the data processing in the four-dye fluorescence detection strategy used in automated DNA sequencing. In this paper, we propose a model to describe the crosstalk phenomenon, and show how the assumptions of the model are supported by experimental data. The crosstalk matrix is estimated via a reparameterization based on a mapping between the distribution of fluorescence intensities and that of dye concentrations. An iterative algorithm is designed to implement the estimation. To evaluate the color-correction quality of a crosstalk matrix, we propose a quantitative measure based on the distribution of the color-corrected data. We illustrate this method by applying it to a sequencing trace of slab gel electrophoresis obtained at the Human Genome Center at Lawrence Berkeley National Laboratory, and that of capillary electrophoresis provided by the Department of Chemistry at UC, Berkeley. The accuracy of this method is also assessed by the bootstrap method.

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Year:  1999        PMID: 10424466     DOI: 10.1002/(SICI)1522-2683(19990601)20:7<1433::AID-ELPS1433>3.0.CO;2-0

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  9 in total

1.  Color-blind fluorescence detection for four-color DNA sequencing.

Authors:  Ernest K Lewis; Wade C Haaland; Freddy Nguyen; Daniel A Heller; Matthew J Allen; Robert R MacGregor; C Scott Berger; Britain Willingham; Lori A Burns; Graham B I Scott; Carter Kittrell; Bruce R Johnson; Robert F Curl; Michael L Metzker
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-30       Impact factor: 11.205

2.  BayesCall: A model-based base-calling algorithm for high-throughput short-read sequencing.

Authors:  Wei-Chun Kao; Kristian Stevens; Yun S Song
Journal:  Genome Res       Date:  2009-08-06       Impact factor: 9.043

3.  Optocoder: computational decoding of spatially indexed bead arrays.

Authors:  Enes Senel; Nikolaus Rajewsky; Nikos Karaiskos
Journal:  NAR Genom Bioinform       Date:  2022-06-07

4.  Quantitative analysis of cardiac tissue including fibroblasts using three-dimensional confocal microscopy and image reconstruction: towards a basis for electrophysiological modeling.

Authors:  Bettina C Schwab; Gunnar Seemann; Richard A Lasher; Natalia S Torres; Eike M Wulfers; Maren Arp; Eric D Carruth; John H B Bridge; Frank B Sachse
Journal:  IEEE Trans Med Imaging       Date:  2013-01-17       Impact factor: 10.048

Review 5.  Model-based quality assessment and base-calling for second-generation sequencing data.

Authors:  Héctor Corrada Bravo; Rafael A Irizarry
Journal:  Biometrics       Date:  2010-09       Impact factor: 2.571

6.  Sequencing error correction without a reference genome.

Authors:  Julie A Sleep; Andreas W Schreiber; Ute Baumann
Journal:  BMC Bioinformatics       Date:  2013-12-18       Impact factor: 3.169

7.  All Your Base: a fast and accurate probabilistic approach to base calling.

Authors:  Tim Massingham; Nick Goldman
Journal:  Genome Biol       Date:  2012-02-29       Impact factor: 13.583

8.  An adaptive decorrelation method removes Illumina DNA base-calling errors caused by crosstalk between adjacent clusters.

Authors:  Bo Wang; Lin Wan; Anqi Wang; Lei M Li
Journal:  Sci Rep       Date:  2017-02-20       Impact factor: 4.379

9.  Swift: primary data analysis for the Illumina Solexa sequencing platform.

Authors:  Nava Whiteford; Tom Skelly; Christina Curtis; Matt E Ritchie; Andrea Löhr; Alexander Wait Zaranek; Irina Abnizova; Clive Brown
Journal:  Bioinformatics       Date:  2009-06-23       Impact factor: 6.937

  9 in total

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