Abstract. Bioinformatics tools are required to produce reliable, high quality data devoid of unwanted sequences in the preprocessing stage of current sequencing and EST projects. In this paper we describe SeqTrim, an algorithm designed to extract the insert sequence from any sequence read devoid of any foreign, contaminant or unwanted sequence, whatever the experimental process was. SeqTrim is easy to install and able to identify the sequence insert by removing low quality sequences, cloning vector, poly A or T tails, adaptors, and sequences that can be considered contaminants. It is easy to use and can be used as stand-alone application or as web page. The default parameters of the algorithm are best suited for most cases but a configurati...
Motivation: Bioinformatics tools, such as assemblers and aligners, are expected to produce more accu...
Background The use of novel algorithmic techniques is pivotal to many important problems in life sci...
Summary: SeqMap is a tool for mapping large amount of short sequences to the genome. It is designed ...
Abstract Background High-throughput automated sequencing has enabled an exponential growth rate of s...
Abstract Background The enormous amount of sequence data available in the public domain database has...
MotivationAccess to biological sequence data, such as genome, transcript, or protein sequence, is at...
Before the SeqAn project, there was clearly a lack of available implementations in sequence analysis...
editing, analysis and storage of long DNA sequences Mats T. Nilsson+ and Gunnar 0. Klein The rapidly...
SEQSEE (SEQuence SEEker) is a multi-purpose, menu-driven suite of programs designed to provide a ful...
Motivation: Sequence analyses oriented to investigate specific features, patterns and functions of p...
Data consistency is necessary for effective bioinformatic analysis. SeqScrub is a web tool that pars...
AbstractContaminant oligonucleotide sequences such as primers and adapters can occur in both ends of...
Background: Many high throughput sequencing (HTS) approaches, such as the Roche/454 platform, produc...
High-throughput sequencing technologies have strongly impacted microbiology, providing a rapid and c...
DNA sequence analysis generates large volumes of data presenting challenging bioinformatic and stati...
Motivation: Bioinformatics tools, such as assemblers and aligners, are expected to produce more accu...
Background The use of novel algorithmic techniques is pivotal to many important problems in life sci...
Summary: SeqMap is a tool for mapping large amount of short sequences to the genome. It is designed ...
Abstract Background High-throughput automated sequencing has enabled an exponential growth rate of s...
Abstract Background The enormous amount of sequence data available in the public domain database has...
MotivationAccess to biological sequence data, such as genome, transcript, or protein sequence, is at...
Before the SeqAn project, there was clearly a lack of available implementations in sequence analysis...
editing, analysis and storage of long DNA sequences Mats T. Nilsson+ and Gunnar 0. Klein The rapidly...
SEQSEE (SEQuence SEEker) is a multi-purpose, menu-driven suite of programs designed to provide a ful...
Motivation: Sequence analyses oriented to investigate specific features, patterns and functions of p...
Data consistency is necessary for effective bioinformatic analysis. SeqScrub is a web tool that pars...
AbstractContaminant oligonucleotide sequences such as primers and adapters can occur in both ends of...
Background: Many high throughput sequencing (HTS) approaches, such as the Roche/454 platform, produc...
High-throughput sequencing technologies have strongly impacted microbiology, providing a rapid and c...
DNA sequence analysis generates large volumes of data presenting challenging bioinformatic and stati...
Motivation: Bioinformatics tools, such as assemblers and aligners, are expected to produce more accu...
Background The use of novel algorithmic techniques is pivotal to many important problems in life sci...
Summary: SeqMap is a tool for mapping large amount of short sequences to the genome. It is designed ...