Bioinformatics Resources

Sequencing Applications through Bioinformatics

Below is a summary of the applications that are avaliable through combining sequencing services with Bioinformatics.



What does it offer?

Starting with genomic DNA you can sequence and assembly a genome with a reference, do de novo assembly for a genome with no reference, while exome sequencing provides an ideal method for looking for variants.


What does it offer?

RNA-seq enables researchers to determine how many and which RNA transcripts are in a cell or sample; it enables identification of DNA sequences in the genome which are copied into RNA and assigned a biological function; and it enables characterization of RNA splicing.


What does it offer?

ChIP (chromatin immunoprecipitation) is used for mapping the in vivo distribution of proteins associated with chromosomal DNA. These proteins can be histone subunits, transcription factors, or other regulatory or structural proteins bound either directly or indirectly to DNA. Using high quality antibodies, protein-interacting regions of chromosomal DNA, as well as their post-translational modifications can be detected.


What will I receive?

The AGRF makes available data in compressed (gzipped) FASTQ format (*.fastq.gz). FASTQ format is a text-based format for storing both a biological sequence and its corresponding quality scores.  For further information on the structure of a FASTQ file see here.  Paired end sequencing generates two files, *R1.fastq.gz for mate 1, *R2.fastq.gz for mate 2.



What does it offer?

Methylation analysis can be genome wide (whole genome bisulfite sequencing), targeted (Illumina HumanMethylation450 BeadChips), promoter and small region specific (Agena) or small region and CpG specific (Qiagen PyroMark)


GO LONG - launching our long read sequencing service!

14 January 2019

We are excited to announce that we will be launching our Long Read Sequencing service on the PacBio platform very soon!

Click to learn more.

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