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Unmapped paired end reads were collected and mapped upon the genomic scaffolds of unmapped sequences from WAB56 104 using BWA mem with the default condition.
6073272 36 bp reads were collected with an average insert length of 400 bp.
Approximately 360 M paired-end reads were collected per lane.
Finally, all mapped reads were collected for further analysis.
The raw FASTQ data files of 151 bp single-end reads were collected for downstream analysis.
The 101 bp reads were collected using the Illumina GA II and sequencing-by-synthesis technology.
Similar(19)
Results for all reads are collected and stored in a text file on HDFS.
These reads are collected in an array for subsequent assembly, thereby limiting the sequence space of the assembly to that of the target region.
36 bp reads are collected on an Illumina Genome Analyzer using sequencing-by-synthesis technology.
In metagenomic projects, millions or billions of DNA or cDNA reads are collected in a single experiment.
After downloading from Metrichor, base-called FAST5 reads are collected in batches of 200 reads and automatically processed in real time by MetaPORE.
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