User guide — cutadapt 1.8 documentation
Kraken: A set of tools for quality control and analysis of high-throughput sequence data☆ | Semantic Scholar
Cutadapt removes adapter sequences from high-throughput sequencing reads - 知乎
Biomolecules | Free Full-Text | High-Throughput Identification of Adapters in Single-Read Sequencing Data
cutPrimers: A New Tool for Accurate Cutting of Primers from Reads of Targeted Next Generation Sequencing | Journal of Computational Biology
Primary Data Analysis of RNA-Seq data| RNA Lexicon
FASTAptameR 2.0: A web tool for combinatorial sequence selections: Molecular Therapy - Nucleic Acids
Quality control & Adapter trimming · Training Course on Next generation sequencing
Open Source at SciLifeLab » cutadapt
High throughput barcoding method for genome-scale phasing | Scientific Reports
Comparison of tools cutting primer sequences from reads with tolerance... | Download Scientific Diagram
Frontiers | An Improved Sequencing-Based Bioinformatics Pipeline to Track the Distribution and Clonal Architecture of Proviral Integration Sites
bio-utils/cutadapt – BioLib
FASTAptamer: A Bioinformatic Toolkit for High-throughput Sequence Analysis of Combinatorial Selections: Molecular Therapy - Nucleic Acids
Cutadapt remoYes adapter sequences from high-throughput sequencing reads Introduction Implementation Features
Biology | Free Full-Text | FLEXBAR—Flexible Barcode and Adapter Processing for Next-Generation Sequencing Platforms
NGS preprocessing - Removing adapters from Fastq reads - Video tutorial - Omics tutorials
Handling of targeted amplicon sequencing data focusing on index hopping and demultiplexing using a nested metabarcoding approach in ecology | Scientific Reports
cutadapt/__main__.py at main · marcelm/cutadapt · GitHub
DNA sequencing - Wikiwand
HaTSPiL: A modular pipeline for high-throughput sequencing data analysis | PLOS ONE
Biomolecules | Free Full-Text | High-Throughput Identification of Adapters in Single-Read Sequencing Data
Quality Control and Preprocessing of Sequencing Reads
De-novo Bacterial draft genome de-novo asembly, from the sequencing machine (Illumina) to a genome database (NCBI) An example case: Assembly of Stenotrophomonas. - ppt download
Trim adapters - Partek® Documentation
RNA-seq with RNase H-based ribosomal RNA depletion specifically designed for C. elegans | microPublication
