Preprocessing: Trimming and filtering reads - YouTube
pTrimmer: An efficient tool to trim primers of multiplex deep sequencing data | BMC Bioinformatics | Full Text
Quality Control and Trimming of NGS sequences - Pseudo Tribulations
A Next Generation Sequencing Short Read Trimmer - Home
Bioinformatics part 2: Processing fastq files for downstream applications - YouTube
Adapter trimming for single end sRNA-seq data. The reads processed by... | Download Scientific Diagram
QIAGEN Bioinformatics Manuals
BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing | Scientific Reports
From next-generation resequencing reads to a high-quality variant data set | Heredity
ClipKIT: A multiple sequence alignment trimming software for accurate phylogenomic inference | PLOS Biology
Adapter Trim | Griffith Lab
Overview of laboratory (A) and bioinformatics workflow (B). | Download Scientific Diagram
FASTQ Quality Assurance Tools - Bioinformatics Team (BioITeam) at the University of Texas - UT Austin Wikis
Skewer: a fast and accurate adapter trimmer for next-generation sequencing paired-end reads – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science
A review of bioinformatic methods for forensic DNA analyses - ScienceDirect
A Bioinformatics Whole-Genome Sequencing Workflow for Clinical Mycobacterium tuberculosis Complex Isolate Analysis, Validated Using a Reference Collection Extensively Characterized with Conventional Methods and In Silico Approaches | Journal of ...
Read QA and Cleaning — Bioinformatics at COMAV 0.1 documentation
Standards and Guidelines for Validating Next-Generation Sequencing Bioinformatics Pipelines: A Joint Recommendation of the Association for Molecular Pathology and the College of American Pathologists - ScienceDirect
Frontiers | A Bioinformatics Pipeline for the Analysis and Target Prediction of RNA Effectors in Bidirectional Communication During Plant–Microbe Interactions
Help with trimming SE reads using dada2- what would you suggest as the best trim/trunc parameters? : r/bioinformatics
de novo assembly of PacBio reads (unix) - Bioinformatics Documentation
JCM | Free Full-Text | Bioinformatics and Computational Tools for Next-Generation Sequencing Analysis in Clinical Genetics
Trimming for RNA-Seq Data: Best Practices and Tools | Basepair
Trimming adapter sequences - is it necessary?
