AlignCode
Tools for analazing
next generation sequencing data
Next-generation sequencing (NGS) technologies have progressive
advantages in terms of cost-effectiveness, unprecedented sequencing
speed, high resolution and accuracy in genomic analyses. To date, these
high-throughput sequencing technologies have been comprehensively
applied in a variety of ways, such as whole genome sequencing, target
sequencing, gene expression profiling, chromatin immunoprecipitation
sequencing, and small RNA sequencing, to accelerate biological and
biomedical research. However, the massive amount of data generated by
NGS represents a great challenge. AlignCode present
guidelines and workflow for data processing, and makes suggestions for
suitable bioinformatics tools used to analyze data for genomics,
transcriptomics and small RNA research.
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