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/pandaseq2962 days ago
YASS :: genomic similarity search tool
...you can specify the seed pattern used in the search step (as provided for example by iedera). Main features of YASS are: multiple, possibly overlapping seeds and a new hit criterion...2936 days ago
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2670 days ago
GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
...nbsp; Meaningful mapping quality. Various alignment strategies (semiglobal bit-vector and Gotoh, anchored). Overlapping of reads for de novo assembly...2535 days ago
miniasm: very fast OLC-based de novo assembler for noisy long reads
...ab. For a C. elegans PacBio data set (only 40X are used, not the whole dataset), miniasm finishes the assembly, including reads overlapping, in ~10 minutes with 16 CPUs....2362 days ago
COPE: an accurate k-mer-based pair-end reads connection tool to facilitate genome assembly
An efficient tool called Connecting Overlapped Pair-End (COPE) reads, to connect overlapping pair-end reads using k-mer frequencies. We evaluated our tool on 30× simulated pair-en...2353 days ago
2203 days ago
EAGLER: a scaffolding tool for long reads.
...created by any NGS assembler and a set of long reads. The long reads are used to extend the contigs present in the NGS draft and possibly join overlapping contigs. EAGLER supports both...2173 days ago