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In genetics and biochemistry, determining the structure of an unbranched biopolymer
biochemistry, sequencing means to determine the primary structure (sometimes incorrectly called the primary sequence) of an unbranched biopolymer. Sequencing results
Sequencing
Process of determining the nucleic acid sequence
DNA sequencing is the process of determining the nucleic acid sequence – the order of nucleotides in DNA. It includes any method or technology that is
DNA_sequencing
Sequencing all the DNA of an individual at once
Whole genome sequencing (WGS), also known as full genome sequencing or just genome sequencing, is the process of determining the entirety of the DNA sequence
Whole_genome_sequencing
International scientific research project (1990–2003)
the base pairs that make up human DNA, and of identifying, mapping and sequencing all of the genes of the human genome from both a physical and a functional
Human_Genome_Project
Sequencing of all the exons of a genome
Exome sequencing, also known as whole exome sequencing (WES), is a genomic technique for sequencing all of the protein-coding regions of genes in a genome
Exome_sequencing
Method of DNA sequencing developed in 1977
Sanger sequencing is a method of DNA sequencing that involves electrophoresis and is based on the random incorporation of chain-terminating dideoxynucleotides
Sanger_sequencing
DNA / RNA sequencing technique
Nanopore sequencing is a third generation approach used in the sequencing of biopolymers — specifically, polynucleotides in the form of DNA or RNA. Nanopore
Nanopore_sequencing
Method used for sequencing random DNA strands
In genetics, shotgun sequencing is a method used for sequencing random DNA strands. It is named by analogy with the rapidly expanding, quasi-random shot
Shotgun_sequencing
Lab technique in cellular biology
RNA-Seq (short for RNA sequencing) is a next-generation sequencing (NGS) technique used to quantify and identify RNA molecules in a biological sample
RNA-Seq
DNA sequencing using the concept of massively parallel processing
Massively parallel sequencing (MPS) is any of several high-throughput approaches to DNA sequencing using the concept of massively parallel processing;
Massively_parallel_sequencing
Examines sequence information from individual cells
Single-cell sequencing examines the nucleic acid sequence information from individual cells with optimized next-generation sequencing technologies, providing
Single-cell_sequencing
Study of genes found in the environment
ecosystems. Metagenomic studies most commonly employ shotgun sequencing though long-read sequencing is being increasingly utilised as technologies advance.
Metagenomics
In electronic circuits that have multiple power supplies, power sequencing is the process of turning power supplies on or off in a particular order and
Power_sequencing
Lab procedure detecting 5-methylcytosines in DNA
Bisulfite sequencing (also known as bisulphite sequencing) is the use of bisulfite treatment of DNA before routine sequencing to determine the pattern
Bisulfite_sequencing
Sequencing by ligation is a DNA sequencing method that uses the enzyme DNA ligase to identify the nucleotide present at a given position in a DNA sequence
Sequencing_by_ligation
Measure of the completeness of DNA sequencing
coverage is one of several measures of the depth or completeness of DNA sequencing, and is more specifically expressed in any of the following terms: Sequence
Coverage_(genetics)
Biochemical method in mass spectrometry
In mass spectrometry, de novo peptide sequencing is the method in which a peptide amino acid sequence is determined from tandem mass spectrometry. Knowing
De_novo_peptide_sequencing
DNA sequencing
Third-generation sequencing (also known as long-read sequencing) is a class of DNA sequencing methods that have the capability to produce substantially
Third-generation_sequencing
Preparation and analysis method for DNA
Duplex sequencing is a library preparation and analysis method for next-generation sequencing (NGS) platforms that employs random tagging of double-stranded
Duplex_sequencing
Methylation process
Reduced representation bisulfite sequencing (RRBS) is an efficient and high-throughput technique for analyzing the genome-wide methylation profiles on
Reduced representation bisulfite sequencing
Reduced_representation_bisulfite_sequencing
In the field of genetic sequencing, genotyping by sequencing, also called GBS, is a method to discover single nucleotide polymorphisms (SNP) in order to
Genotyping_by_sequencing
Method used to analyze protein interactions with DNA
CUT&Tag-sequencing, also known as cleavage under targets and tagmentation, is a method used to analyze protein interactions with DNA. CUT&Tag-sequencing combines
CUT&Tag_sequencing
Whole genome bisulfite sequencing is a next-generation sequencing technology used to determine the DNA methylation status of single cytosines by treating
Whole genome bisulfite sequencing
Whole_genome_bisulfite_sequencing
DNA sequencing method
Illumina dye sequencing is a technique used to determine the series of base pairs in DNA, also known as DNA sequencing. The reversible terminated chemistry
Illumina_dye_sequencing
Laboratory technique
Patch-sequencing (patch-seq) is a modification of patch-clamp technique that combines electrophysiological, transcriptomic and morphological characterization
Patch-sequencing
Biological theory
DNA sequencing theory is the broad body of work that attempts to lay analytical foundations for determining the order of specific nucleotides in a sequence
DNA_sequencing_theory
Linked-read sequencing, a type of DNA sequencing technology, uses specialized technique that tags DNA molecules with unique barcodes before fragmenting
Linked-read_sequencing
Transposon insertion sequencing (Tn-seq) combines transposon insertional mutagenesis with massively parallel sequencing (MPS) of the transposon insertion
Transposon_sequencing
Cancer genome sequencing is the whole genome sequencing of a single, homogeneous or heterogeneous group of cancer cells. It is a biochemical laboratory
Cancer_genome_sequencing
Sequencing by hybridization is a class of methods for determining the order in which nucleotides occur on a strand of DNA. Typically used for looking for
Sequencing_by_hybridization
Method used to analyze protein interactions with DNA
CUT&RUN sequencing, also known as cleavage under targets and release using nuclease, is a method used to analyze protein interactions with DNA. CUT&RUN
CUT&RUN_sequencing
Topics referred to by the same term
Sequencing may refer to: DNA sequencing Whole genome sequencing This disambiguation page lists articles associated with the title Genetic sequencing.
Genetic_sequencing
Method of analysis of genetic material
Clinical metagenomic next-generation sequencing (mNGS) is the comprehensive analysis of microbial and host genetic material (DNA or RNA) in clinical samples
Clinical metagenomic sequencing
Clinical_metagenomic_sequencing
DNA sequencing method
Ion semiconductor sequencing is a method of DNA sequencing based on the detection of hydrogen ions that are released during the polymerization of DNA.
Ion_semiconductor_sequencing
American biotechnology company
manufactures systems for high-throughput DNA sequencing. The company is noted for developing a sequencing instrument that it claims can sequence a complete
Ultima_Genomics
MicroRNA sequencing (miRNA-seq), a type of RNA-Seq, is the use of next-generation sequencing or massively parallel high-throughput DNA sequencing to sequence
MicroRNA_sequencing
DNA sequencing method
cloning and sequencing efforts in plants, fungi, and mammals with minor alterations. This technique, also known as "directed sequencing," employs a series
Primer_walking
Scientific instrument that automates the DNA sequencing process
A DNA sequencer is a scientific instrument used to automate the DNA sequencing process. Given a sample of DNA, a DNA sequencer is used to determine the
DNA_sequencer
DNA sequencing technology
DNA nanoball sequencing (DNBSEQ) is a high throughput sequencing technology that is used to determine the entire genomic sequence of an organism. The
DNA_nanoball_sequencing
Discipline in genetics
cells. Genomics also involves the sequencing and analysis of genomes through uses of high throughput DNA sequencing and bioinformatics to assemble and
Genomics
Sequencing of amino acid arrangement in a protein
Protein sequencing is the practical process of determining the amino acid sequence of all or part of a protein or peptide. This may serve to identify the
Protein_sequencing
Method used to analyze protein interactions with DNA
ChIP-sequencing, also known as ChIP-seq, is a method used to analyze protein interactions with DNA. ChIP-seq combines chromatin immunoprecipitation (ChIP)
ChIP_sequencing
Species of mammal of Asia
Bactrian Camels Genome Sequencing and Analysis Consortium provides a C. bactrianus ferus genome using next generation sequencing. Several effective population
Bactrian_camel
Complete set of nucleic acid sequences for humans
reported the sequencing of 88% of human genome, but as of 2020, at least 8% was still missing. In 2021, scientists reported sequencing a complete, female
Human_genome
Device or software that records, edits or plays back musical notes
mixing-automation in DAWs, and software effect or instrument plug-ins for DAWs with sequencing features Audio data in audio sequencers including DAWs, loop-based music
Music_sequencer
Scientific technique used in analysing DNA
Polony sequencing is an inexpensive but highly accurate multiplex sequencing technique that can be used to “read” millions of immobilized DNA sequences
Polony_sequencing
Method of DNA sequencing
Maxam–Gilbert sequencing is a method of DNA sequencing developed by Allan Maxam and Walter Gilbert in 1976–1977. This method is based on nucleobase-specific
Maxam–Gilbert_sequencing
Computational analysis of large, complex sets of biological data
sequence tag (EST) sequencing, serial analysis of gene expression (SAGE) tag sequencing, massively parallel signature sequencing (MPSS), RNA-Seq, also
Bioinformatics
Massive parallel signature sequencing (MPSS) is a procedure that is used to identify and quantify mRNA transcripts, resulting in data similar to serial
Massively parallel signature sequencing
Massively_parallel_signature_sequencing
American biotechnology company
systems for gene sequencing and some novel real time biological observation.[failed verification] PacBio has two principal sequencing platforms: single-molecule
Pacific_Biosciences
DNA sequencing method
Circular consensus sequencing (CCS) is a DNA sequencing method that is used in conjunction with single-molecule real-time sequencing to yield highly accurate
Circular_consensus_sequencing
Team in advertising that means predefining a particular sequence of a series of creatives
Creative sequencing is a term in advertising that means predefining a particular sequence (sequencing) of a series of creatives (creative), usually under
Creative_sequencing
Chinese biotechnology company
company that has developed and commercialized a DNA sequencing platform for human genome sequencing and analysis. Complete Genomics was founded in June
Complete_Genomics
The principle of solid phase DNA sequencing was described in 1989 based on binding of biotinylated DNA to streptavidin-coated magnetic beads and elution
Solid_phase_sequencing
Type of activated sludge process for the treatment of wastewater
Sequencing batch reactors (SBR) or sequential batch reactors are a type of activated sludge process for the treatment of wastewater. SBRs treat wastewater
Sequencing_batch_reactor
Sequencing by Oligonucleotide Ligation and Detection (SOLiD) is a DNA sequencing technology developed by Life Technologies and has been available since
ABI_Solid_Sequencing
Positional sequencing is a method of sequencing DNA that simultaneously generates information about both identity and location of nucleotide sequences
Positional_sequencing
Topics referred to by the same term
Gene sequencing may refer to: DNA sequencing, the process of determining the nucleic acid sequence – the order of nucleotides in DNA Whole genome sequencing
Gene_sequencing
Molecular biology sequencing technique
Fiber-seq is a molecular biology multiplexed sequencing assay capturing genomic and epigenomic information for individual chromatin fibers. It achieves
Fiber-Seq
DNA testing for endangerment assessment
Genome sequencing of endangered species is the application of Next Generation Sequencing (NGS) technologies in the field of conservation biology, with
Genome sequencing of endangered species
Genome_sequencing_of_endangered_species
classifying reads from a DNA sequencing experiment. For example, in metagenomic studies it is important to be able to tell if a sequencing read belongs to a new
Bloom filters in bioinformatics
Bloom_filters_in_bioinformatics
Single-molecule sequencing technology
Transmission electron microscopy DNA sequencing is a single-molecule sequencing technology that uses transmission electron microscopy techniques. The method
Transmission electron microscopy DNA sequencing
Transmission_electron_microscopy_DNA_sequencing
Phonological principle observed in many languages
The sonority sequencing principle (SSP) or sonority sequencing constraint is a phonotactic principle that aims to explain or predict the structure of
Sonority_sequencing_principle
British biochemist (1918–2013)
in Cambridge, he developed and subsequently refined the first-ever DNA sequencing technique, which vastly expanded the number of feasible experiments in
Frederick_Sanger
Measurement in DNA sequencing
by automated DNA sequencing. It was originally developed for the computer program Phred to help in the automation of DNA sequencing in the Human Genome
Phred_quality_score
In DNA sequencing, a read is an inferred sequence of base pairs (or base pair probabilities) corresponding to all or part of a single DNA fragment. A typical
Read_(biology)
Small RNA sequencing (Small RNA-Seq) is a type of RNA sequencing based on the use of NGS technologies that allows to isolate and get information about
Small_RNA_sequencing
German company
company specialist in DNA and RNA sequencing for academic and industrial partners worldwide. The company offered sequencing and bioinformatics solutions from
GATC_Biotech
Fluorescent in situ sequencing (FISSEQ) is a method of sequencing a cell's RNA while it remains in tissue or culture using next-generation sequencing. FISSEQ combines
Fluorescent in situ sequencing
Fluorescent_in_situ_sequencing
Methods of compressing data tailored specifically for genomic data
In genomics, DNA sequencing is the process of converting information stored in nucleic acid into digital data that can be stored inside computers, and
Compression of genomic sequencing data
Compression_of_genomic_sequencing_data
American biotechnology company
The company provides a line of products and services that serves the sequencing, genotyping and gene expression, and proteomics markets, and serves more
Illumina,_Inc.
American scientist and entrepreneur
He is best known for his contributions to genomics, semiconductor DNA sequencing, and personalized medicine. Avantome was acquired by Illumina in 2008
Helmy_Eltoukhy
Method for immune repertoire sequencing
TCR-Seq (T-cell Receptor Sequencing) is a method used to identify and track specific T cells and their clones. TCR-Seq utilizes the unique nature of a
Tcr-seq
Method for sequencing DNA
Single-molecule real-time (SMRT) sequencing is a parallelized single molecule DNA sequencing method. Single-molecule real-time sequencing utilizes a zero-mode waveguide
Single-molecule real-time sequencing
Single-molecule_real-time_sequencing
Sequences remaining within RNA after RNA splicing
untranslated regions of messenger RNA (mRNA), and coding regions. Exome sequencing has proven to be an efficient method of determining the genetic basis
Exome
Method of sequencing amino acids in a peptide
Edman degradation, developed by Pehr Edman, is a method of sequencing amino acids in a peptide. In this method, the amino-terminal residue is labeled and
Edman_degradation
Degradome sequencing (Degradome-Seq), also referred to as parallel analysis of RNA ends (PARE), is a modified version of 5'-Rapid Amplification of cDNA
Degradome_sequencing
Branch of genomics concerned with the genome of an individual
genomics or consumer genetics is the branch of genomics concerned with the sequencing, analysis and interpretation of the genome of an individual. The genotyping
Personal_genomics
Set of overlapping DNA segments that together represent a consensus region of DNA
region of DNA. In bottom-up sequencing projects, a contig refers to overlapping sequence data (reads); in top-down sequencing projects, contig refers to
Contig
All genetic material of an organism
the vast majority of nucleotides are identical between individuals, but sequencing multiple individuals is necessary to understand the genetic diversity
Genome
various sequencing technologies to achieve the task of assembling a genome from fragmented, sequenced DNA resulting from shotgun sequencing. Genome assembly
Hybrid_genome_assembly
Discipline of human genetics
analyzing and interpreting individualized genetic information by genome sequencing to identify genetic variations compared to the library of known sequences
Personalized_genomics
American geneticist (born 1928–2008)
sequencing, earlier than the Frederick Sanger's method in 1975 and Walter Gilbert's chemical procedure in 1977. Wu's contributions on DNA sequencing are
Ray_Wu
Branch of biology that studies biological systems at the molecular level
level. Molecular biologists today have access to increasingly affordable sequencing data at increasingly higher depths, facilitating the development of novel
Molecular_biology
Describes the rate of DNA sequencing or cost per sequenced base as a function of time
The Carlson curve is a term to describe the rate of DNA sequencing or cost per sequenced base as a function of time. It is the biotechnological equivalent
Carlson_curve
American company
company based in San Francisco, California. It offers a whole-genome sequencing service. Nebula Genomics was co-founded in 2018 by George Church, geneticist
Nebula_Genomics
American scientist and entrepreneur (born 1963)
American scientist and entrepreneur notable for his contributions to DNA sequencing. He resides in Miami, Florida. Rothberg was born in New Haven, Connecticut
Jonathan_Rothberg
Genetic characteristic of tumorous tissue
genomic sequence, and its measurement has been enabled by next generation sequencing. High TMB and DNA damage repair mutations were discovered to be associated
Tumor_mutational_burden
(short for single cell genome and transcriptome sequencing) is a novel form of single-cell sequencing technique allowing one to simultaneously obtain
G&T-seq
DNA sampled from the environment rather than directly from an individual organism
skin, carcasses and hair. Samples can be analyzed by high-throughput DNA sequencing methods, known as metagenomics, metabarcoding, and single-species detection
Environmental_DNA
Topics referred to by the same term
High-throughput biology, a cell biology concept High-throughput sequencing, DNA sequencing Measuring data throughput, a communications concept Throughput
High-throughput
The Baylor College of Medicine Human Genome Sequencing Center (BCM-HGSC) was established by Richard A. Gibbs in 1996 when Baylor College of Medicine was
Human Genome Sequencing Center
Human_Genome_Sequencing_Center
Technique in molecular biology
Chromatin Interaction Analysis by Paired-End Tag Sequencing (ChIA-PET or ChIA-PETS) is a technique in molecular biology that incorporates chromatin immunoprecipitation
ChIA-PET
American population genomics company
applications created by approved partners. Helix handles sample collection, DNA sequencing, and secure data storage and partners develop on-demand products. Helix
Helix_(genomics_company)
Magnetic sequencing is a single-molecule sequencing method in development. A DNA hairpin, containing the sequence of interest, is bound between a magnetic
Single-molecule magnetic sequencing
Single-molecule_magnetic_sequencing
Laboratory technique for DNA methylation profiling
TET-assisted pyridine borane sequencing or TAPS is a laboratory technique in epigenetics for high-throughput profiling of DNA methylation at a single base-pair
TET-assisted pyridine borane sequencing
TET-assisted_pyridine_borane_sequencing
Indian Consortium to study and monitor COVID-19 genome sequencing
Government of India on 30 December 2020, to study and monitor genome sequencing and virus variation of circulating strains of COVID-19 in India. Initially
INSACOG
U.K.-based nanopore sequencing company
technology for the real-time analysis of DNA and RNA. Its platform includes sequencing devices, consumables and software used across research, applied and clinical
Oxford_Nanopore_Technologies
Era of predictive and personalized medicine
of predictive and personalized medicine during which the cost of fully sequencing an individual's genome (WGS) is roughly one thousand USD. It is also the
$1,000_genome
Study of lichen taxonomy and evolution
revolutionized in recent decades by molecular biology and genomics. DNA sequencing now allows researchers to resolve cryptic species and deep evolutionary
Lichen_systematics
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