At 1010Genome, we are passionate about the incredible potential that lies within the genetic code of every living organism. Our mission is to empower researchers, clinicians, and organizations with cutting-edge bioinformatics solutions to decode, analyze, and understand the wealth of information hidden within the DNA.
Who we are
1010Genome is a leading bioinformatic company specializing in Next-Generation Sequencing (NGS) data analysis. With a team of highly skilled bioinformaticians, geneticists, and computational biologists, we provide comprehensive solutions for genomic research and clinical applications. We are dedicated to helping you make sense of the vast and complex genomic data generated by NGS technologies.
Check out our skills:
NGS Data Analysis
We offer a wide range of NGS data analysis services, from preprocessing and quality control to variant calling and structural variant analysis. Our state-of-the-art pipelines ensure accurate and reliable results.
WGS & Exome SNP Analysis
Identify SNPs, InDels, CNVs and Structural variants in genome & exome datasets. Our tools and expertise assist you in identifying single nucleotide polymorphisms (SNPs), insertions, deletions, and other structural variants.
RNA Seq / Gene Expression
Understand gene expression and regulation with our transcriptomic analysis services. We help you decipher RNA-Seq data to gain insights into gene function, alternative splicing, and more.
16s rRNA Profiling & Metagenomics
Dive into the microbial world with metagenomic analysis. Whether you're studying the microbiome, environmental samples, or infectious diseases, we provide in-depth analysis to answer your questions.
Genome Assembly & Annotation
Unleash the true potential of your genomic data with our Genome Assembly Services. Whether you opt for Long-Read or Short-Read Sequencing, our commitment to precision and excellence empowers you to explore the depths of your genetic blueprint.
Structural Variant Analysis
Identify structural variations in genomes that cause a disease or result into unique phenotype using short and long NGS data.
Identify Biological Pathways enriched in a gene list from RNA Seq and sequencing data. Interpretation and visualization of statistically enriched pathways.
ChIP Seq Analysis
Accelerate your ChIP-seq analysis with 1010Genome's analysis service. Uncover valuable insights into chromatin dynamics efficiently and precisely.
Need bioinformatics consultation for project design? We design projects and help with custom bioinformatics development.