High-throughput sequencing

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• High throughput cell biology — is the combination of cell biology with automation to address questions from the scale of a single cell to the human Genome. It permits questions to be addressed that are otherwise unattainable using conventional methods. It exploits optics,… …   Wikipedia

• Sequencing — For the sense of sequencing used in electronic music, see the music sequencer article. For sequence learning in cognitive science, see sequence learning. In genetics and biochemistry, sequencing means to determine the primary structure (sometimes …   Wikipedia

• DNA sequencing — Part of a series on Genetics Key components Chromosome DNA • RNA Genome Heredity Mutation Nucleotide Variation …   Wikipedia

• Full genome sequencing — Genome sequencing redirects here. For the sequencing only of DNA, see DNA sequencing. An image of the 46 chromosomes, making up the diploid genome of human male. (The mitochondrial chromosome is not shown.) Full genome sequencing (FGS), also… …   Wikipedia

• Massive parallel sequencing — is a term used to describe several revolutionary approaches to DNA sequencing, the so called next generation sequencing (NGS) technologies or second generation sequencing. These sequencing technologies have emerged in late 1996 [1][2] an have… …   Wikipedia

• Microfluidic Sanger sequencing — The completion of the Human Genome Project has been a cornerstone in the advancement of biological studies. The outcomes of obtaining a complete reference map (including the sequence) of the human genome have ushered in the post genome era of… …   Wikipedia

• DNA nanoball sequencing — is a high throughput sequencing technology that is used to determine the entire genomic sequence of an organism. The method uses rolling circle replication to amplify small fragments of genomic DNA into DNA nanoballs. Fluorescent probes bind to… …   Wikipedia

• Degradome sequencing — (Degradome Seq),[1][2] also referred to as parallel analysis of RNA ends (PARE),[1][2] is a modified 5 rapid amplification of cDNA ends (RACE) with high throughput deep sequencing (SBS) method. Degradome sequencing provides a comprehensive means… …   Wikipedia

• Bisulfite sequencing — Figure 1: Outline of bisulfite conversion of sample sequence of genomic DNA. Nucleotides in blue are unmethylated cytosines converted to uracils by bisulfite, while red nucleotides are 5 methylcytosines resistant to conversion …   Wikipedia

• DNA-encoded chemical library — DNA encoded chemical libraries (DEL) are a new technology for the synthesis and screening of collections of chemical compounds of unprecedented size and quality. DEL represents an advance in medicinal chemistry which bridges the fields of… …   Wikipedia

• Methylated DNA immunoprecipitation — (MeDIP or mDIP) is a large scale (chromosome or genome wide) technique that is used to enrich for methylated DNA sequences. It consists of isolating methylated DNA fragments via an antibody raised against 5 methylcytosine (5mC). This technique… …   Wikipedia