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Journal ArticleDOI

Applications of next-generation sequencing to phylogeography and phylogenetics

TLDR
In this article, the authors outline some of the major obstacles specific to the application of NGS to phylogeography and phylogenetics, including the focus on non-model organisms, the necessity of obtaining orthologous loci in a cost-effective manner, and the predominate use of gene trees in these fields.
About
This article is published in Molecular Phylogenetics and Evolution.The article was published on 2013-02-01. It has received 586 citations till now. The article focuses on the topics: Phylogenomics.

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Citations
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DnaSP 6: DNA Sequence Polymorphism Analysis of Large Data Sets.

TL;DR: The DNA Sequence Polymorphism (DnaSP) software as mentioned in this paper is a popular tool for performing exhaustive population genetic analyses on multiple sequence alignments, such as single and multi-locus coalescent simulations under a wide range of demographic scenarios.
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Stacks: an analysis tool set for population genomics

TL;DR: The expanded population genomics functions in Stacks will make it a useful tool to harness the newest generation of massively parallel genotyping data for ecological and evolutionary genetics.
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How to fail at species delimitation.

TL;DR: Researchers should apply a wide range of species delimitation analyses to their data and place their trust in delimitations that are congruent across methods, for in most contexts it is better to fail to delimit species than it is to falsely delimit entities that do not represent actual evolutionary lineages.
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High-Throughput Genomic Data in Systematics and Phylogenetics

TL;DR: This review presents recent advances in laboratory methods for collection of high-throughput phylogenetic data and challenges and constraints for phylogenetic analysis of these data, and offers recommendations for the most promising protocols and data-analysis workflows currently available.
Journal ArticleDOI

AMAS: a fast tool for alignment manipulation and computing of summary statistics.

TL;DR: AMAS (Alignment Manipulation And Summary), a tool that can be used either as a stand-alone command-line utility or as a Python package, works on amino acid and nucleotide alignments and combines capabilities of sequence manipulation with a function that calculates basic statistics.
References
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The Sequence Alignment/Map format and SAMtools

TL;DR: SAMtools as discussed by the authors implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments.
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Fast and accurate short read alignment with Burrows–Wheeler transform

TL;DR: Burrows-Wheeler Alignment tool (BWA) is implemented, a new read alignment package that is based on backward search with Burrows–Wheeler Transform (BWT), to efficiently align short sequencing reads against a large reference sequence such as the human genome, allowing mismatches and gaps.
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Inference of population structure using multilocus genotype data

TL;DR: Pritch et al. as discussed by the authors proposed a model-based clustering method for using multilocus genotype data to infer population structure and assign individuals to populations, which can be applied to most of the commonly used genetic markers, provided that they are not closely linked.
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Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

TL;DR: Bowtie extends previous Burrows-Wheeler techniques with a novel quality-aware backtracking algorithm that permits mismatches and can be used simultaneously to achieve even greater alignment speeds.
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AFLP: a new technique for DNA fingerprinting.

TL;DR: The AFLP technique provides a novel and very powerful DNA fingerprinting technique for DNAs of any origin or complexity that allows the specific co-amplification of high numbers of restriction fragments.
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