SECAPR—a bioinformatics pipeline for the rapid and user-friendly processing of targeted enriched Illumina sequences, from raw reads to alignments

T Andermann, Á Cano, A Zizka, C Bacon, A Antonelli - PeerJ, 2018 - peerj.com
Evolutionary biology has entered an era of unprecedented amounts of DNA sequence data,
as new sequencing technologies such as Massive Parallel Sequencing (MPS) can generate …

Targeted sequence capture as a powerful tool for evolutionary analysis1

CE Grover, A Salmon, JF Wendel - American journal of botany, 2012 - Wiley Online Library
Next‐generation sequencing technologies (NGS) have revolutionized biological research by
significantly increasing data generation while simultaneously decreasing the time to data …

Xenomapper: mapping reads in a mixed species context

MJ Wakefield - Journal of Open Source Software, 2016 - joss.theoj.org
Xenomapper is a utility for post processing mapped DNA sequencing reads that have been
aligned to a primary genome and a secondary genome, and binning reads into species …

Natrix: a Snakemake-based workflow for processing, clustering, and taxonomically assigning amplicon sequencing reads

M Welzel, A Lange, D Heider, M Schwarz… - BMC …, 2020 - Springer
Background Sequencing of marker genes amplified from environmental samples, known as
amplicon sequencing, allows us to resolve some of the hidden diversity and elucidate …

A bioinformatic platform to integrate target capture and whole genome sequences of various read depths for phylogenomics

P G. Ribeiro, MF Torres Jiménez… - Molecular …, 2021 - Wiley Online Library
The increasing availability of short‐read whole genome sequencing (WGS) provides
unprecedented opportunities to study ecological and evolutionary processes. Although loci …

Comparison of short-read sequence aligners indicates strengths and weaknesses for biologists to consider

R Musich, L Cadle-Davidson, MV Osier - Frontiers in Plant Science, 2021 - frontiersin.org
Aligning short-read sequences is the foundational step to most genomic and transcriptomic
analyses, but not all tools perform equally, and choosing among the growing body of …

ReadTools: A universal toolkit for handling sequence data from different sequencing platforms

D Gómez‐Sánchez, C Schlötterer - Molecular ecology …, 2018 - Wiley Online Library
Sequencing whole genomes has become a standard research tool in many disciplines
including Molecular Ecology, but the rapid technological advances in combination with …

IM-TORNADO: a tool for comparison of 16S reads from paired-end libraries

P Jeraldo, K Kalari, X Chen, J Bhavsar, A Mangalam… - PloS one, 2014 - journals.plos.org
Motivation 16S rDNA hypervariable tag sequencing has become the de facto method for
accessing microbial diversity. Illumina paired-end sequencing, which produces two separate …

[HTML][HTML] Target sequence capture of Barnadesioideae (Compositae) demonstrates the utility of low coverage loci in phylogenomic analyses

P de Lima Ferreira, R Batista, T Andermann… - Molecular Phylogenetics …, 2022 - Elsevier
Target sequence capture has emerged as a powerful method to sequence hundreds or
thousands of genomic regions in a cost-and time-efficient approach. In most cases, however …

New alignment-based sequence extraction software (ALiBaSeq) and its utility for deep level phylogenetics

A Knyshov, ERL Gordon, C Weirauch - PeerJ, 2021 - peerj.com
Despite many bioinformatic solutions for analyzing sequencing data, few options exist for
targeted sequence retrieval from whole genomic sequencing (WGS) data with the ultimate …