Split multiple fastq files by matching barcodes in one or more of the sequence files. Barcodes in the tab-delimited barcodes.txt file are matched against the beginning (or end) of the specified index read(s). By default, barcodes must match exactly, but --mistmatches can be set higher if desired. Compressed input is read (from all files) if the first input file name ends in .gz. Reading of compressed input can be forced with the gzipin option.</p
Partial fastq dataset associated with RAD42 barcode file. Combine with RAD42-2 prior to analysis
Barcode files (Individual sample names and associated barcode/molecular identifier) associated with ...
Applying a cutoff for barcode abundance eliminates most recall of longer barcodes that were not inte...
Split multiple fastq files by matching barcodes in one or more of the sequence files. Barcodes in th...
A zip archive of seven text files containing sample names and associated barcodes for demultiplexing...
This file contains raw ONT reads (fast5 files) for the first sample (barcode 1, sample name INF042) ...
Raw: Barcode sequence data, sorted by index and trimmed but not filtered; Filtering_pipeline: Pipeli...
Example of a tab-delimited table containing the information to connect barcodes to samples in differ...
<p>To assign an Illumina read to a particular sample, one examines both of the barcodes at each end ...
Partial fastq dataset associated with RAD22 barcode file. Combine with RAD22-1 prior to analysis
Barcode metadata file (one barcode per individual fecal sample) corresponding to "BEHAVBUGS_NoIndex_...
This release provides a new feature that allows users to further customize the barcodes based on the...
Partial fastq dataset associated with RAD22 barcode file. Combine with RAD22-2 prior to analysis
Quantitative and systems biology approaches benefit from the unprecedented depth of next-generation ...
New version of LR-splitpipe: demultiplex.py Improves performance on larger sets of reads by reading...
Partial fastq dataset associated with RAD42 barcode file. Combine with RAD42-2 prior to analysis
Barcode files (Individual sample names and associated barcode/molecular identifier) associated with ...
Applying a cutoff for barcode abundance eliminates most recall of longer barcodes that were not inte...
Split multiple fastq files by matching barcodes in one or more of the sequence files. Barcodes in th...
A zip archive of seven text files containing sample names and associated barcodes for demultiplexing...
This file contains raw ONT reads (fast5 files) for the first sample (barcode 1, sample name INF042) ...
Raw: Barcode sequence data, sorted by index and trimmed but not filtered; Filtering_pipeline: Pipeli...
Example of a tab-delimited table containing the information to connect barcodes to samples in differ...
<p>To assign an Illumina read to a particular sample, one examines both of the barcodes at each end ...
Partial fastq dataset associated with RAD22 barcode file. Combine with RAD22-1 prior to analysis
Barcode metadata file (one barcode per individual fecal sample) corresponding to "BEHAVBUGS_NoIndex_...
This release provides a new feature that allows users to further customize the barcodes based on the...
Partial fastq dataset associated with RAD22 barcode file. Combine with RAD22-2 prior to analysis
Quantitative and systems biology approaches benefit from the unprecedented depth of next-generation ...
New version of LR-splitpipe: demultiplex.py Improves performance on larger sets of reads by reading...
Partial fastq dataset associated with RAD42 barcode file. Combine with RAD42-2 prior to analysis
Barcode files (Individual sample names and associated barcode/molecular identifier) associated with ...
Applying a cutoff for barcode abundance eliminates most recall of longer barcodes that were not inte...