The increasingly widespread use of next generation sequencing protocols has brought the need for the development of user-friendly raw data processing tools. Here, we explore 2FAST2Q, a versatile and intuitive standalone program capable of extracting and counting feature occurrences in FASTQ files. Despite 2FAST2Q being previously described as part of a CRISPRi-seq analysis pipeline, in here we further elaborate on the program's functionality, and its broader applicability and functions. 2FAST2Q is built in Python, with published standalone executables in Windows MS, MacOS, and Linux. It has a familiar user interface, and uses an advanced custom sequence searching algorithm. Using published CRISPRi datasets in which Escherichia coli and Myco...
High-throughput DNA sequencing produces vast amounts of data, with millions of short reads that usua...
SSR_pipeline is a flexible set of programs designed to efficiently identify simple sequence repeats ...
The collection consists of RNA sequencing (RNA-seq) datasets in fastq format which were used to eval...
The increasingly widespread use of next generation sequencing protocols has brought the need for the...
BackgroundRNA sequencing (RNA-seq) has become the standard means of analyzing gene and transcript ex...
Abstract Background Next generation sequencing datasets are stored as FASTQ formatted files. In orde...
FAST (FAST Analysis of Sequences Toolbox) provides simple, powerful open source command-line tools t...
<div><p>The presence of duplicates introduced by PCR amplification is a major issue in paired short ...
Here, we describe a tool suite that functions on all of the commonly known FASTQ format variants and...
Analysis of CRISPR-induced mutations at targeted locus can be achieved by polymerase chain reaction ...
The presence of duplicates introduced by PCR amplification is a major issue in paired short reads fr...
The presence of duplicates introduced by PCR amplification is a major issue in paired short reads fr...
Next Generation Sequencing machines are generating mil-lions of short DNA sequences (reads) everyday...
<div><p>Pipelines for the analysis of Next-Generation Sequencing (NGS) data are generally composed o...
CRISPR interference (CRISPRi) is a powerful tool to link essential and nonessential genes to specifi...
High-throughput DNA sequencing produces vast amounts of data, with millions of short reads that usua...
SSR_pipeline is a flexible set of programs designed to efficiently identify simple sequence repeats ...
The collection consists of RNA sequencing (RNA-seq) datasets in fastq format which were used to eval...
The increasingly widespread use of next generation sequencing protocols has brought the need for the...
BackgroundRNA sequencing (RNA-seq) has become the standard means of analyzing gene and transcript ex...
Abstract Background Next generation sequencing datasets are stored as FASTQ formatted files. In orde...
FAST (FAST Analysis of Sequences Toolbox) provides simple, powerful open source command-line tools t...
<div><p>The presence of duplicates introduced by PCR amplification is a major issue in paired short ...
Here, we describe a tool suite that functions on all of the commonly known FASTQ format variants and...
Analysis of CRISPR-induced mutations at targeted locus can be achieved by polymerase chain reaction ...
The presence of duplicates introduced by PCR amplification is a major issue in paired short reads fr...
The presence of duplicates introduced by PCR amplification is a major issue in paired short reads fr...
Next Generation Sequencing machines are generating mil-lions of short DNA sequences (reads) everyday...
<div><p>Pipelines for the analysis of Next-Generation Sequencing (NGS) data are generally composed o...
CRISPR interference (CRISPRi) is a powerful tool to link essential and nonessential genes to specifi...
High-throughput DNA sequencing produces vast amounts of data, with millions of short reads that usua...
SSR_pipeline is a flexible set of programs designed to efficiently identify simple sequence repeats ...
The collection consists of RNA sequencing (RNA-seq) datasets in fastq format which were used to eval...