QIAGEN Bioinformatics Manuals
Illumina Adapter Sequence (Illumina Inc) | Bioz | Ratings For Life-Science Research
Duplex sequencing - Wikipedia
Trimming adapter sequences - is it necessary?
Titration-free 454 sequencing using Y adapters | Nature Protocols
High-Throughput, Amplicon-Based Sequencing of the CREBBP Gene as a Tool to Develop a Universal Platform-Independent Assay | PLOS ONE
Biotech7005 | The practical material from the course Biotech 7005: Bioinformatics and Systems Modelling
PEAT – paired-end sequencing adapter trimming algorithm | RNA-Seq Blog
Schematic for adapter and primer design for the two rare cutters EcoRI and PstI and the frequent cutter MseI | Learn Science at Scitable
phylogenetics - Why do NEB adapters have non-complementary sequence? - Bioinformatics Stack Exchange
The MGH NextGen Sequencing Core | Core Services
How to trim adapters from miRNA data sequenced on Illumina machine?
Tomato Epigenome Database
QC Fail Sequencing » Read-through adapters can appear at the ends of sequencing reads
AdapterStripping Right - Array Suite Wiki
Adapter trimming: Why are adapter sequences trimmed from only the 3' ends of reads - Illumina Knowledge
LUMI-PCR: an Illumina platform ligation-mediated PCR protocol for integration site cloning, provides molecular quantitation of integration sites | Mobile DNA | Full Text
Adapter trimming: Why are adapter sequences trimmed from only the 3' ends of reads - Illumina Knowledge
When do you strictly need to know the adapter sequence to trim NGS data?
What are paired-end reads? – The Sequencing Center
How short inserts affect sequencing performance - Illumina Knowledge
TUFTS - TUCF Genomics
Biomolecules | Free Full-Text | High-Throughput Identification of Adapters in Single-Read Sequencing Data
Sequencing Knowledge Base – CZ Biohub at Stanford
Reference genome-independent assessment of mutation density using restriction enzyme-phased sequencing | BMC Genomics | Full Text
Development of Coupling Controlled Polymerizations by Adapter-ligation in Mate-pair Sequencing for Detection of Various Genomic Variants in One Single Assay | bioRxiv
