Results for "PANDASEQ"
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PAired-eND Assembler for DNA sequences
PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence. More at https://github.com/neufeld/pandaseq2932 days ago
- PANDASEQ assembles paired-end Illumina reads into sequences, trying to correct for err...ases, and user-supplied modules. http://neufeldserver.uwaterloo.ca/~apmasell/pandaseq_man1.html
2640 days ago
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Genome Assembly Tools and Software - PART1 !!
...d De Novo Assembler HyDA is a multipurpose assembler, particularly tested for single cell and normal multicell genome co-assembly PANDASEQ 2.8 / Pandaseq-sam 1.3 – PAired-eND As...2667 days ago
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Linux operating system aimed at scientists
...that a problem that was preventing the desktop to not start on VirtualBox has been fixed, the QIIME and Bowtie-Bio tools have been upgraded, the pandaseq paired end assembler has been...3375 days ago
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PAired-eND Assembler for DNA sequences
PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence. More at https://github.com/neufeld/pandaseqTags: Bioinformatics, NGS, Assembly, Paired-End, PANDASEQ, Illumina
2932 days ago
- PANDASEQ assembles paired-end Illumina reads into sequences, trying to correct for errors and uncalled bases. The assembler reads two files in FASTQ format with quality information. If amplification primers were used (e.g., to isolate a variable region of the 16S gene, or the constant regions aro...
Tags: Bioinformatics, Assembly, PANDASEQ, Genome, NGS, Illumina
2640 days ago
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