Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Flavia J. Krsticevic

dblp:179/2231 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2017
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › synthetic biology › oligonucleotide design
barcode design
0.312017
Designing robust watermark barcodes for multiplex long-read sequencing · Bioinform. 2017
Bioinformatics and computational biology › single-cell analysis › single-cell data preprocessing
demultiplexing
0.312017
Designing robust watermark barcodes for multiplex long-read sequencing · Bioinform. 2017
Bioinformatics and computational biology
sequence analysis
0.312017
Designing robust watermark barcodes for multiplex long-read sequencing · Bioinform. 2017

Methods — techniques the papers use, named apart from their topics

insertion-deletion-substitution error modeling · 0.3error-correcting code design · 0.3
YearPublicationVenuePosition
2017 Designing robust watermark barcodes for multiplex long-read sequencing
abstract
Motivation: To attain acceptable sample misassignment rates, current approaches to multiplex single-molecule real-time sequencing require upstream quality improvement, which is obtained from multiple passes over the sequenced insert and significantly reduces the effective read length. In order to fully exploit the raw read length on multiplex applications, robust barcodes capable of dealing with the full single-pass error rates are needed. Results: We present a method for designing sequencing barcodes that can withstand a large number of insertion, deletion and substitution errors and are suitable for use in multiplex single-molecule real-time sequencing. The manuscript focuses on the design of barcodes for full-length single-pass reads, impaired by challenging error rates in the order of 11%. The proposed barcodes can multiplex hundreds or thousands of samples while achieving sample misassignment probabilities as low as 10-7 under the above conditions, and are designed to be compatible with chemical constraints imposed by the sequencing process. Availability and Implementation: Software tools for constructing watermark barcode sets and demultiplexing barcoded reads, together with example sets of barcodes and synthetic barcoded reads, are freely available at www.cifasis-conicet.gov.ar/ezpeleta/NS-watermark . Contact: [email protected].
Joaquín Ezpeleta, Flavia J. Krsticevic, Pilar Bulacio, Elizabeth Tapia
Bioinform.2