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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]
Following this lawsuit, 10x Genomics discontinued their linked-read assay. [15] An exception was made for linked-read products which had already been sold by the company prior to the lawsuit, allowing 10x Genomics to continue to provide those researchers with services such as support and warranty maintenance for this technology. [citation needed]
Previous efforts of coupling index-sorting measurements from single cell sorts with scRNA-seq were limited to running a small sample size and were not compatible with multiplexing and massive parallel high-throughput sequencing. CITE-seq has been shown to be compatible with high-throughput microfluidic platforms like 10X Genomics and Drop-seq ...
10x or 10X may refer to: 10x Management, an American talent management company; 10x Genomics, an American biotechnology company; Windows 10X, an abandoned edition of Microsoft's operating system; A grade of powdered sugar fineness; Zeolite 10X, a calcium-type molecular sieve with faujasite framework structure
[7] [5] Since its development, many various protocols of whole genome bisulfite sequencing have been developed aiming to improve the efficiency and efficacy of its single-base mapping. As the costs of next-generation sequencing have decreased, whole genome bisulfite sequencing has become more widely used in clinical and experimental research. [ 3 ]
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Easy protocol steps have been shown to drive complete denaturation. Ensuring the usage of small fragments via shearing or digestion, fresh reagents, and sufficient denaturing time is crucial for complete denaturing [ 5 ] Another suggested technique is to carry out the bisulfite reaction at 95 °C although DNA degradation also occurs at high ...
Protocols requiring DNA amplification are often cumbersome to implement and may introduce sequencing errors. The preparation of single-molecule templates is more straightforward and does not require PCR, which can introduce errors in the amplified templates.