Deriving confidence intervals for mutation rates across a wide range of evolutionary distances using FracMinHash

MR Hera, NT Pierce-Ward, D Koslicki - Genome research, 2023 - genome.cshlp.org
Sketching methods offer computational biologists scalable techniques to analyze data sets
that continue to grow in size. MinHash is one such technique to estimate set similarity that …

A comparative evaluation of hybrid error correction methods for error-prone long reads

S Fu, A Wang, KF Au - Genome biology, 2019 - Springer
Background Third-generation sequencing technologies have advanced the progress of the
biological research by generating reads that are substantially longer than second …

Accurate self-correction of errors in long reads using de Bruijn graphs

L Salmela, R Walve, E Rivals, E Ukkonen - Bioinformatics, 2017 - academic.oup.com
Motivation New long read sequencing technologies, like PacBio SMRT and Oxford
NanoPore, can produce sequencing reads up to 50 000 bp long but with an error rate of at …

Objective review of de novo stand‐alone error correction methods for NGS data

AS Alic, D Ruzafa, J Dopazo… - Wiley Interdisciplinary …, 2016 - Wiley Online Library
The sequencing market has increased steadily over the last few years, with different
approaches to read DNA information prone to different types of errors. Multiple studies …

Debiasing fracminhash and deriving confidence intervals for mutation rates across a wide range of evolutionary distances

MR Hera, T Pierce, D Koslicki - bioRxiv, 2022 - biorxiv.org
Sketching methods offer computational biologists scalable techniques to analyze data sets
that continue to grow in size. MinHash is one such technique to estimate set similarity that …

Toll protein family structure, evolution and response of the whiteleg shrimp (Litopenaeus vannamei) to exogenous iridescent virus

H Liu, S Guo, Y He, Q Shi, M Yang… - Journal of Fish …, 2021 - Wiley Online Library
Whiteleg shrimp is a widely cultured crustacean, but frequent disease outbreaks have
decreased production and caused significant losses. Toll‐like receptors (TLRs) comprise a …

A hybrid and scalable error correction algorithm for indel and substitution errors of long reads

AK Das, S Goswami, K Lee, SJ Park - BMC genomics, 2019 - Springer
Background Long-read sequencing has shown the promises to overcome the short length
limitations of second-generation sequencing by providing more complete assembly …

LRCstats, a tool for evaluating long reads correction methods

S La, E Haghshenas, C Chauve - Bioinformatics, 2017 - academic.oup.com
Motivation Third-generation sequencing (TGS) platforms that generate long reads, such as
PacBio and Oxford Nanopore technologies, have had a dramatic impact on genomics …

Efficient hybrid De novo error correction and assembly for long reads

M Kchouk, M Elloumi - 2016 27th International workshop on …, 2016 - ieeexplore.ieee.org
The new generation of long reads generated by Oxford nanopore sequencing technology
has revolutionized the next generation sequencing environment with the appearance of its …

An error correction and DeNovo assembly approach for nanopore reads using short reads

M Kchouk, M Elloumi - Current Bioinformatics, 2018 - ingentaconnect.com
Background: Error Correction is an important task in the analysis and manipulations of NGS
data. The purpose of error correction is to facilitate data analysis for large projects like de …