PEARis a paired-end reads merger for the Illumina platform. PEARevaluates all possible paired-end read overlaps and does not require the target fragment size as input. It also implements a statistical test for minimizing false-positive results. The highly optimized and parallelized implementation allo...
There already exist tools for merging these paired-end reads when the target fragments are equally long. However, when fragment lengths vary and, in particular, when either the fragment size is shorter than a single-end read, or longer than twice the size of a single-end read, most state-...
Motivation: The Illumina paired-end sequencing technology can generate reads from both ends of target DNA fragments, which can subsequently be merged to increase the overall read length. There already exist tools for merging these paired-end reads when the target fragments are equally long. However...
<description>Paired-End read merger</description> <macros> <token name="@TOOL_VERSION@">0.9.6</token> <token name="@VERSION_SUFFIX@">2</token> <token name="@VERSION_SUFFIX@">3</token> <xml name="format_action"> <actions> <conditional name="library.type"> <when value="paired"> <...
摘要: Motivation: The Illumina paired-end sequencing technology can generate reads from both ends of target DNA fragments, which can subsequently be merged to increase the overall read length. There alr ...关键词: Staphylococcus aureus Sequence Alignment Sequence Analysis, DNA Genomics Software High-...