BIOINFORMATICS
our services
basics
Base calling is the process of assigning bases to different peaks of the sequencer lecture.
We provide demultiplexed data and high quality FASTQ files
Reads are ‘cleaned’ to improve average quality and reduce the volume of erroneous data
Genome annotation is the process of identifying regions of interest in a DNA/RNA sequence in order to assign specific information about structure or function
Genome mapping is a technique used to assign the location of a particular gene on a chromosome and measure their relative locations and distances between genes
SNPs (single nucleotide polymorphisms) or Indels (insertions or deletions) mapped to a physical location in the reference genome
Transcriptome de novo assembly is the process by which one uses RNA-Seq data to assemble a transcriptome without a reference genome
Intermediate
advanced
DGE involves the measurement of genes whose expression differ according to phenotype or experimental conditions
Metagenomic analysis involves the application of bioinformatics tools to study the genetic material from environmental, uncultured microorganisms
Single nucleotide polymorphisms, structural variants and copy number variation are discovered in the genome by comparing several genome sequences across multiple individuals
Fast, inexpensive and accurate
We are dedicated to provide the most efficient bioinformatics analysis
our expertise
Genomics
We can provide you state-of-the-art genomic sequencing with latest bioinformatics analytical tools
Metagenomics
Every known pathogen (bacteria, viruses, fungus & nematodes) could be rapidly detect through metagenomics
SEQUENCING TECHONOLOGIEs
Being experts in every types of sequencing technologies allows us to provide analysis for every needs