We provide cost effective sequencing services for various next generation sequencing platforms – Illumina, Ion Torrent,
PacBio and Sanger.
We provide data analysis services for all Next Generaton Sequencing (NGS) platform that include Illumina, Ion Torrent and Pacbio.
Robust Exome sequencing data analysis pipelines to identify SNPs, INDELS, CNV and other structural variants
Identify diffrentially expressed genes, generate transcriptome assembly and study alternative spilicing events across samples with our suite of bioinformatics pipelines.
Generate high quality genome assembly ready for annotaion. We expertise in short read, long read or hybrid as per project demands.
Comprehensive biodiversity analysis to identify taxa and species of bacterial, fungal and archae present in metagenomic samples from soil, water or clinical sournces.
Explore the diversity and fucntions of microbes present in samples. Robust pipelines for shotgun metagenomics assembly, identify genes and pathways in environmental or clinical samples.
Use our robust pipelines to identify structural variants – INDELS, CNVs and STRs using short reads or long reads data for your genomic studies.
We provide customized bioinformatics services that include programming, data analysis and publication writting
Recent advancement in next generation sequencing strategies has lead us to great advancement of transcriptome studies. Various techniques for transcriptome analysis are available and widely used since development of microarray technology and sequencing of the human genome. mRNA level measurements…
RNA sequencing (RNA seq), also called whole transcriptome shotgun sequencing, uses next-generation sequencing (NGS) to reveal the presence and quantity of RNA in a biological sample at a given time. The correct identification of differentially expressed genes (DEGs) between specific…
It may sometimes be hard to imagine the costs of certain procedures or actions dropping to 0.01 percentage of costs over a period of ten years. In 2008, whole genome sequencing cost upwards of a staggering 10 million dollars; this…
From the time of Hippocrates, medical research has always focused on understanding the person who suffers from ailments. Hippocrates famously said – ‘it is far more important to know what person the disease has, than what disease the person has’….
DNA sequencing costs are typically compared on the basis of the cost of determining one mega base of DNA sequence and the cost of human-sized genome sequencing. The primary reasons for a change in pricing is largely due to the…
The transcripts or gene readouts that form the transcriptome are central to the activity of building and maintaining cells. An RNA sequence shows the exact sequence of the DNA, and the analysis of the sequence helps in determining the exact…
1010Genome offers next generation sequencing data analysis through Illumina sequencing platform. The cost effective, optimized solutions for whole exome sequencing are critical for complex disease studies to discover SNP biomarkers. Similarly, Illumina sequencing is a very time and cost effective…
While the costs towards most data analysis and genome sequencing have crashed considerably, there is a need to ensure that cost reduction is never achieved at the cost of compromised quality. This is of paramount importance. The process of whole…
For those who have non-medical background, exome sequencing is a method of studying an individual’s exome which account for about 85% of medical conditions and maladies that affect a person in his or her lifetime. It adopts a target sequencing…
RNA sequencing, also referred to as RNA-Seq is a next-generation sequencing process with focus on study of total RNA content of a organism or tissue. RNA sequencing is done to analyze the cellular transcriptome which is continuously changing in its…
