1010Genome Public group

1010Genome is a sequencing and bioinformatics data analysis service provider. Our portfolio of services includes: Whole genome, exome, RNA-seq, cancer genomics and metagenomics sequencing and data analysis.

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We offer quick and high quality next-generation sequencing data analysis and bioinformatics services.

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We offer quick and high quality next-generation sequencing data analysis and bioinformatics services.

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The study of RNAs content and sum total of RNA transcripts is called transcriptomics. Transcriptomics is easy with fairly straightforward library preparation and reproducible results. Contact 1010Genome for Transcriptomics RNA Seq Analysis.

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Illumina sequencing also known as sequencing by synthesis (SBS) sequencing is the most popular next-generation technology. Illumina sequencing the most cost effective next-generation sequencing technology for most of the applications. Visit Illumina sequencing workflow at 1010 Genome.

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Gene Mapping refers to the determination of the relative positions of genes on a DNA molecule. Genome annotation to build a genetic map. Get in touch with us today for consultation about your differential gene expression project.

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Metagenomics provides an opportunity to simultaneously explore two aspects of a microbial community who is there and what are they capable of doing? Contact 1010Genome today for the consultation about your Shotgun Metagenomics project.

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RNA-Seq is a revolutionising transcriptome studies. It is highly sensitive, precise and accurate tool for measuring abundances and expression across transcriptomes. Hit 1010Genome for RNA Sequencing services.

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16s rRNA sequencing has been established for the identification and taxonomic classification of bacterial species. Get in touch with us today for consultation about microbiome analysis and 16s rRNA sequencing analysis.

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The analysis of gene expression microarray data, especially the use of linear models for analysing designed experiments and the assessment of differential expression.

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Whole-genome sequencing provides a comprehensive view of entire genome. WGS or genome resequencing are ideally suited for genome wide variant identifications and structural variation detection.

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