A comparison of tools for the simulation of genomic next-generation sequencing data

M Escalona, S Rocha, D Posada - Nature Reviews Genetics, 2016 - nature.com
Computer simulation of genomic data has become increasingly popular for assessing and
validating biological models or for gaining an understanding of specific data sets. Several …

Simulating Illumina metagenomic data with InSilicoSeq

H Gourlé, O Karlsson-Lindsjö, J Hayer… - …, 2019 - academic.oup.com
Motivation The accurate in silico simulation of metagenomic datasets is of great importance
for benchmarking bioinformatics tools as well as for experimental design. Users are …

NanoSim: nanopore sequence read simulator based on statistical characterization

C Yang, J Chu, RL Warren, I Birol - GigaScience, 2017 - academic.oup.com
Abstract Background The MinION sequencing instrument from Oxford Nanopore
Technologies (ONT) produces long read lengths from single-molecule sequencing–valuable …

[HTML][HTML] The challenges of designing a benchmark strategy for bioinformatics pipelines in the identification of antimicrobial resistance determinants using next …

A Angers-Loustau, M Petrillo, J Bengtsson-Palme… - …, 2018 - ncbi.nlm.nih.gov
Abstract Next-Generation Sequencing (NGS) technologies are expected to play a crucial
role in the surveillance of infectious diseases, with their unprecedented capabilities for the …

CAMISIM: simulating metagenomes and microbial communities

A Fritz, P Hofmann, S Majda, E Dahms, J Dröge… - Microbiome, 2019 - Springer
Background Shotgun metagenome data sets of microbial communities are highly diverse,
not only due to the natural variation of the underlying biological systems, but also due to …

Simulation of nanopore sequencing signal data with tunable parameters

H Gamaarachchi, JM Ferguson… - Genome …, 2024 - genome.cshlp.org
In silico simulation of high-throughput sequencing data is a technique used widely in the
genomics field. However, there is currently a lack of effective tools for creating simulated …

SimLoRD: simulation of long read data

BK Stöcker, J Köster, S Rahmann - Bioinformatics, 2016 - academic.oup.com
Motivation: Third generation sequencing methods provide longer reads than second
generation methods and have distinct error characteristics. While there exist many read …

Draft genome of the Northern snakehead, Channa argus

J Xu, C Bian, K Chen, G Liu, Y Jiang, Q Luo… - Giga …, 2017 - academic.oup.com
Abstract Background The Northern snakehead (Channa argus), a member of the Channidae
family of the Perciformes, is an economically important freshwater fish native to East Asia. In …

VISOR: a versatile haplotype-aware structural variant simulator for short-and long-read sequencing

D Bolognini, A Sanders, JO Korbel, A Magi… - …, 2020 - academic.oup.com
VISOR is a tool for haplotype-specific simulations of simple and complex structural variants
(SVs). The method is applicable to haploid, diploid or higher ploidy simulations for bulk or …

Transcript-targeted analysis reveals isoform alterations and double-hop fusions in breast cancer

S Namba, T Ueno, S Kojima, K Kobayashi… - Communications …, 2021 - nature.com
Although transcriptome alteration is an essential driver of carcinogenesis, the effects of
chromosomal structural alterations on the cancer transcriptome are not yet fully understood …