Results 241 to 250 of about 308,842 (252)

CNV_IFTV: An Isolation Forest and Total Variation-Based Detection of CNVs from Short-Read Sequencing Data

IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2021
Xiguo Yuan, Jiaao Yu, Jianing Xi
exaly  

Mucosal Microbiome in Patients with Early Bowel Polyps: Inferences from Short-Read and Long-Read 16S rRNA Sequencing

Cancers, 2023
Alexander F Engel, Mark P Molloy
exaly  

Quality-score guided error correction for short-read sequencing data using CUDA

Procedia Computer Science, 2010
Bertil Schmidt, Weiguo Liu, Wolfgang Müller-Wittig   +2 more
exaly  

A Short-Read Multiplex Sequencing Method for Reliable, Cost-Effective and High-Throughput Genotyping in Large-Scale Studies

Human Mutation, 2013
Anders Krogh, Karsten Kristiansen, Jun Wang   +2 more
exaly  

Viral population analysis and minority-variant detection using short read next-generation sequencing

Philosophical Transactions of the Royal Society B: Biological Sciences, 2013
Simon J Watson, Matthijs R A Welkers, Daniel P Depledge   +2 more
exaly  

ResSeq: Enhancing Short-Read Sequencing Alignment By Rescuing Error-Containing Reads

IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2015
Weixing Feng, , Fenglin Cao
exaly  

Elucidating the coordination of RNA processing using short-read and long-read RNA-sequencing methods

Nature Reviews Molecular Cell Biology
CARLOS Alfonso-Gonzalez, Valerie Hilgers   +1 more
exaly  

Using the Velvet de novo Assembler for Short‐Read Sequencing Technologies

Current Protocols in Bioinformatics, 2010
Daniel R Zerbino
exaly  

2022: A Wild Year for Short Reads in Genome Sequencing?

GEN Biotechnology, 2022
openaire   +1 more source

A Comparison of Structural Variant Calling from Short-Read and Nanopore-Based Whole-Genome Sequencing Using Optical Genome Mapping as a Benchmark

Genes
Yang Pei, Melanie Tanguy, Adam Giess
exaly