TagGD: Fast and Accurate Software for DNA Tag Generation and Demultiplexing | PLOS ONE
Index Adapters Pooling Guide (1000000041074)
Not all sequence tags are created equal: designing and validating sequence identification tags robust to indels. - Abstract - Europe PMC
Index Adapters Pooling Guide (1000000041074)
PDF) DeML: Robust demultiplexing of Illumina sequences using a likelihood-based approach
PDF) DeML: Robust demultiplexing of Illumina sequences using a likelihood-based approach
Not All Sequence Tags Are Created Equal: Designing and Validating Sequence Identification Tags Robust to Indels | PLOS ONE
Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing | Nature Genetics
QIAGEN Bioinformatics Manuals
Index Adapters Pooling Guide (1000000041074)
Index Adapters Pooling Guide (1000000041074)
PDF) Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing
Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing | BMC Genomics | Full Text
Multiplexed Competition in a Synthetic Squid Light Organ Microbiome Using Barcode-Tagged Gene Deletions | mSystems
Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing | Nature Genetics
TagGD: Fast and Accurate Software for DNA Tag Generation and Demultiplexing | PLOS ONE
Index Adapters Pooling Guide (1000000041074)
TagGD: Fast and Accurate Software for DNA Tag Generation and Demultiplexing | PLOS ONE
CRISPRi-seq for genome-wide fitness quantification in bacteria | Nature Protocols
Identifying chromatin features that regulate gene expression distribution | Scientific Reports
Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing | BMC Genomics | Full Text
CUTseq is a versatile method for preparing multiplexed DNA sequencing libraries from low-input samples | Nature Communications
