1010 Genome
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Next Generation Sequencing & Bioinformatics Analysis

NGS Sequencing Services

  • We deliver fast quality sequencing services at affordable rates across multiple next generation sequencing platforms
  • Access to Illumina, Ion Torrent, Pacbio, Oxford Nanopore and Sanger sequencer
  • Expertise in Next Generation Sequencing DNA extraction & library preparation
  • Optimized protocols for NGS short read and long reads sequencing
  • Expert advice on DNA/RNA extraction from bacteria, fungi, plants, biofilms and difficult environmental samples.

Advance Bioinformatics Data Analysis

  • 1010 Genome provides quality affordable bioinformatics data analysis services to research, clinical and biotech industry
  • Variant Identification – Quality analysis with low false positive / negative SNPs and INDELS
  • Differential Gene Expression – Tailored analysis based on  experiment design
  • Genome Assembly – Accurate and high quality ready to annotate assemblies for short reads, long reads or hybrid assemblies.
  • Metagenomics – Discover the biodiversity and gene pathways in your metagenomics samples
  • Custom Bioinformatics Analysis – Custom data analysis for tailored to your project requirements

Services

NGS Sequencing Services Portfolio

We provide cost effective sequencing services for various next generation sequencing platforms – Illumina, Ion Torrent,
PacBio and Sanger.

Whole Genome Sequencing

We provide data analysis services for all Next Generaton Sequencing (NGS) platform that include Illumina, Ion Torrent and Pacbio.

Whole Exome Sequencing

Robust Exome sequencing data analysis pipelines to identify SNPs, INDELS, CNV and other structural variants

RNA Sequencing / Gene Expression

Identify diffrentially expressed genes, generate transcriptome assembly and study alternative spilicing events across samples with our suite of bioinformatics pipelines.

Genome Assembly & Annotation

Generate high quality genome assembly ready for annotaion. We expertise in short read, long read or hybrid as per project demands.

16s rRNA Metagenomics

Comprehensive biodiversity analysis to identify taxa and species of bacterial, fungal and archae present in metagenomic samples from soil, water or clinical sournces.

Shotgun Metagenomics

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.

Structural Variation Analysis

Use our robust pipelines to identify structural variants – INDELS, CNVs and STRs using short reads or long reads data for your genomic studies.

Custom Bioinformatics Services

We provide customized bioinformatics services that include programming, data analysis and publication writting

Why work with us?

We offer quick and high quality next-generation sequencing data analysis and bioinformatics services. Our dedicated team of experts work with you at every phase of project to deliver optimal results for your research and clinical studies. A team of bioinformaticians and computer scientists are constantly working to build advance data analysis pipeline to deliver best sequencing and bioinformatics data analysis results to you.

  • Dedicated experts
  • Well defined process
  • Support for all NGS platforms
  • High quality results
  • Bioinformatics data analysis pipeline
  • World Class computational infrastructure
  • Bioinformatics Expertise
  • Data Security
  • Post project support

Latest News

Structural Variation identification in Breast Cancer with Whole Genome Sequencing using Long reads

blog1, PacBio, Whole Genome Sequencing

doi: https://doi.org/10.1101/847855 Link: https://www.biorxiv.org/content/biorxiv/early/2019/11/19/847855.full.pdf Advancement of high throughput sequencing technologies have enabled researchers to identify or screen cancer causing structural variants. Long-read, single molecule sequencing technologies from Pacific Biosciences (PacBio) and Oxford Nanopore Technologies (ONT) have been shown as most reliable…

Next Generation Sequencing reveals transcriptional analysis of Masson Pine (Pinus massoniana) under High CO2 Stress

blog1, Next Generation Sequencing, RNA Sequencing, Transcriptome Analysis

Link: https://www.mdpi.com/2073-4425/10/10/804/htm Citation: Genes 2019, 10(10), 804; https://doi.org/10.3390/genes10100804 Masson pine (Pinus massoniana) is a conifer species distributed in 17 provinces, autonomous regions and municipalities located south of the Qinling Mountains in China. It thrives in a warm and humid climate, growing in arid,…

Next Generation 16s rRNA analysis assessing Potentially Active Bacteria and Foodborne Pathogens.

16s rRNA sequencing, blog1, Next Generation Sequencing

Citation: 16 September 2019 / Accepted: 27 September 2019 / Published: 11 October 2019 Link: https://www.mdpi.com/2304-8158/8/10/480/htm In recent years advancement in high throughput next generation sequencing has enabled researchers to detect the entire bacterial diversity/biodiversity spectra and foodborne pathogens in…

The Pomegranate (Punica granatum L.) draft de novo genome assembly explores genetic divergence between soft and hard seeded cultivars

blog1, de novo genome assembly

In this study, researcher’s generated a high‐quality and long‐range contiguity chromosome‐scale de novo genome assembly of the soft‐seeded pomegranate cultivar ‘Tunisia’ with the help of pacbio long reads sequencing and high‐throughput chromosome conformation capture techniques. Re-sequencing of 26 pomegranate varieties…

De novo Transcriptome Assembly and Differential Gene Expression analysis Identify Drought Resistant genes in Cynanchum thesioides (Xerophytic shrubs)

blog1, RNA Sequencing, Transcriptome Analysis

RNA sequencing (RNA Seq) is revolutionizing the study of the transcriptomes. Highly sensitive and accurate tool for measuring expression across the transcriptome, RNA Seq provides researchers with visibility into previously undetected changes occurring in disease states, in response to therapeutics,…

RNA Seq Identifies signatures in Biliary Atresia pediatric samples missed by traditional histopathology or serum liver malfunction markers

blog1, RNA Sequencing, Transcriptome Analysis

Transcriptome analysis by next-generation sequencing (RNA-seq) allows investigation of a transcriptome at unsurpassed resolution. One major benefit is that RNA-seq analysis is independent of a priori knowledge on the sequence under investigation, thereby also allowing analysis of poorly characterized Plasmodium species. Several RNA Seq pipelines are developed for…

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