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  2. Single-cell sequencing - Wikipedia

    en.wikipedia.org/wiki/Single-cell_sequencing

    Genome (DNA) sequencing. Single-cell DNA genome sequencing involves isolating a single cell, amplifying the whole genome or region of interest, constructing sequencing libraries, and then applying next-generation DNA sequencing (for example Illumina, Ion Torrent). Single-cell DNA sequencing has been widely applied in mammalian systems to study ...

  3. 10x Genomics - Wikipedia

    en.wikipedia.org/wiki/10x_Genomics

    10x Genomics was founded in 2012 by Serge Saxonov, Ben Hindson and Kevin Ness to create advanced testing equipment for use in cellular biology. [3] Prior to starting the company, Saxonov was the founding architect, and director of research and development at 23andMe. [2] Ness left 10x Genomics in December 2016 [4] and in 2018, Justin McAnear ...

  4. Spatial transcriptomics - Wikipedia

    en.wikipedia.org/wiki/Spatial_transcriptomics

    The 10X Genomics Visium assay is a newer and improved version of the Spatial Transcriptomics assay. ... high-throughput single cell sequencing and an existing ...

  5. CITE-Seq - Wikipedia

    en.wikipedia.org/wiki/CITE-Seq

    CITE-Seq. CITE-Seq (C ellular I ndexing of T ranscriptomes and E pitopes by Seq uencing) is a method for performing RNA sequencing along with gaining quantitative and qualitative information on surface proteins with available antibodies on a single cell level. [1] So far, the method has been demonstrated to work with only a few proteins per cell.

  6. Single-cell transcriptomics - Wikipedia

    en.wikipedia.org/wiki/Single-cell_transcriptomics

    Single-cell transcriptomics examines the gene expression level of individual cells in a given population by simultaneously measuring the RNA concentration (conventionally only messenger RNA (mRNA)) of hundreds to thousands of genes. [1] Single-cell transcriptomics makes it possible to unravel heterogeneous cell populations, reconstruct cellular ...

  7. Linked-read sequencing - Wikipedia

    en.wikipedia.org/wiki/Linked-read_sequencing

    The raw sequencing data is then processed through bioinformatics (e.g., the GemCode analysis software developed by 10x Genomics) to remove low-quality reads and to assign reads to their respective barcodes. [2] Reads can be aligned to a reference genome or assembled de novo to generate long-range contigs.

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