AT Rich Sequence

Base Sequence

Base Composition

Molecular Sequence Data

GC Rich Sequence

DNA

Transcription, Genetic

Tornado outbreak sequence of May 2019

Epitranscriptomic sequencing

Exome sequencing

Whole genome sequencing

Patch-sequencing

Tornado outbreak sequence of May 2003

The Simpsons opening sequence

Sequence learning

Sequences 72 & 73

Sylvester's sequence

Sequence analysis in social sciences

Low-discrepancy sequence

Deterministic Barcoding in Tissue for Spatial Omics Sequencing

Tornado outbreak sequence of March 24-28, 2021

List of sequence alignment software

Whole genome bisulfite sequencing

Single-cell DNA template strand sequencing

Sequence (musical form)

Cambridge Reference Sequence

Sonority Sequencing Principle

Limit of a sequence

Moser-de Bruijn sequence

Longest linear sequence

MicroRNA sequencing

Nanopore sequencing

Human Genome Sequencing Center

List of sequenced plastomes

Shotgun sequencing

Main sequence

De novo peptide sequencing

Genome4

• Led by the National Human Genome Research Institute (NHGRI), a team of researchers at the National Institute of Standards and Technology (NIST) and many other organizations used advanced sequencing technologies to read out the full DNA sequence of the Y chromosome - a region of the genome that typically drives male reproductive development. (nist.gov)
• Last year, a team from the Telomere-to-Telomere (T2T) consortium, which is made up of experts from dozens of organizations such as NIST, generated the most complete reference genome at the time by using new sequencing technologies to crack previously indecipherable regions of the genome. (nist.gov)
• Importantly, we need to advance genome sequencing and oxygen production at national level and to build regional capacities for vaccine production. (who.int)
• Complete Genome Sequence of Cyanobacterium Geminocystis sp. (bvsalud.org)

Exome2

• Background De novo mutations are emerging as an important cause of neurocognitive impairment, and whole exome sequencing of case-parent trios is a powerful way of detecting them. (bmj.com)
• Methods The Deciphering Developmental Disorders study is using whole exome sequencing in family trios to investigate children with severe, sporadic, undiagnosed developmental delay. (bmj.com)

Genomes2

• Using them both as guides for sequencing a diverse group of over 1,200 separate genomes, they found that T2T-Y drastically improved the outcomes. (nist.gov)
• COVID-19-compatible symptoms, and symptomatic HCP sequencing demonstrated that SARS-CoV-2 viral genomes were sent home per MDH and CDC guidance. (cdc.gov)

Nucleotide4

• quence typing with nucleotide sequence typing of 3 antigen The clonal complex distribution of 171 isolates collected genes increased the discriminatory index achieved from in New South Wales, Australia ( 8 ), was distinct from the 0.975 to 0.992 among 620 clinical isolates from Oxford- shire, United Kingdom. (cdc.gov)
• ST catenated nucleotide sequences of the MLST loci, which butions of different transmission routes are poorly quanti- indicated that the Australian dataset was 3.6% differenti- fi ed. (cdc.gov)
• Nucleotide sequence-based isolate characterization shire dataset: 575 (98.6% of isolates) fl aA SVR sequences methods such as multilocus sequence typing (MLST) suc- contained 130 distinct SVR alleles, and 567 (97.1%) fl aB cessfully catalog bacterial pathogens and provide a rational, sequences contained 111 SVR alleles. (cdc.gov)
• Examples of this kind of meta data are secondary structures (RNA and protein), protein hydrophobicity assignments, or other alternative alphabets for polypeptides, sequence quality data and nucleotide alignments with translations. (metacpan.org)

Fragment1

• They examined the sample with a combination of cutting-edge technologies - namely high fidelity and nanopore sequencing - that make the DNA fragment puzzle pieces larger and thus easier to assemble. (nist.gov)

Genetic2

• The results of a study published in Nature demonstrate that this advance improves DNA sequencing accuracy for the chromosome, which could help identify certain genetic disorders and potentially uncover the genetic roots of others. (nist.gov)
• DNA sequencing isn't as simple as reading genetic material from a genome's beginning to its end. (nist.gov)

Protein1

• It phosphorylates a specific sequence on protein targets. (news-medical.net)

Data2

• The length of the meta data sequence is not dependent on the amount of the meta information. (metacpan.org)
• We encourage all countries to enhance sequencing capacity and data sharing. (who.int)

Benchmarks1

• The GIAB's mission is to produce test materials, or benchmarks, that can be used to evaluate sequencing technologies or methods. (nist.gov)

Absent1

• The researchers pitted their complete Y chromosome sequence, named T2T-Y, against the most widely used reference genome's Y chromosome parts, which are riddled with stretches of absent code. (nist.gov)

Molecule1

• Conserved region 2 (CR2) is a serine-rich region that functions as a hinge on the molecule. (news-medical.net)

Implementation1

• Meta provides basic, pure perl implementation of sequences with meta information. (metacpan.org)

Study2

• This study aims to use high-throughput sequencing (HTS) and ion chromatography to determine: the compositions of the microbial communities ("microbiomes") present in the port and their changes over a year, understand how water chemistry changes may correlate with changes in the microbial composition, and determine which harmful human and marine pathogens are present in the port. (nova.edu)
• Case 4 was a phenotypically isolated case recruited into an undiagnosed rare disorders sequencing study. (bmj.com)

Method3

• The materials themselves are highly accurate readouts of specific genes that can act as an answer key for checking the results of a particular sequencing method. (nist.gov)
• Prefix sub , like in subseq(), means that the method applies to sub region of the sequence range and takes start and end as arguments. (metacpan.org)
• Prefix named_ in method names allows the used to attach multiple meta strings to one sequence by explicitly naming them. (metacpan.org)

Region1

• Our Region is rich with human resources, knowledge, and research capacities. (who.int)

Code1

• So, researchers and clinicians rely on special software to piece together fragments of sequenced code in the correct order like a puzzle. (nist.gov)

Length1

• Since it is dependent on the length of the sequence, it needs to be manipulated after the sequence. (metacpan.org)

Complete2

• The development of high-throughput DNA sequencing (also commonly referred to as "Next Generation") techniques have allowed for a more complete characterization of marine microbes to be obtained. (nova.edu)
• If the range is not defined, it defaults to the complete sequence. (metacpan.org)

Important1

• Hidden inside this sequence is another important number in mathematics: the golden ratio. (pagosasun.com)

Made2

• Amid some very troubling allegations made against Rick and Morty co-creator Justin Roiland, Adult Swim has decided to continue the animated series without him - which will mean casting a new voice actor! (comicbookmovie.com)
• James Lewis said that Dick Gammage had made "excellent points" at the last meeting, which Mr. Lewis believed were "focused" and "on target" especially with regards to technical issues. (cdc.gov)

Genomic2

• This Funding Opportunity Announcement (FOA), issued by the National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, encourages applications that propose to perform replication, fine-mapping, and sequencing studies of human genomic regions that are putatively associated with phenotypes relevant to the NIAMS mission. (nih.gov)
• Oxford Nanopore's technology can, with very high accuracy, read any length of native DNA, enabling the identification and comprehensive sequence assessment of genomic insertion sites without the risk of missing off target integrations that may negatively impact the therapeutic or the patient. (businesswire.com)

Centers2

• The Large-Scale DNA Sequencing Project continues this tradition by directing multiple population studies and participant samples through two sequencing centers to streamline data analysis and avoid repetition. (nih.gov)
• This limited competition RFA will use the U54 cooperative agreement mechanism to continue the effort of supporting human microbiome sequencing that was begun in FY07 through funds provided to NHGRI- and NIAID-funded large-scale sequencing centers. (nih.gov)

Proteins2

• The amino acid sequences of fifty-five LRR proteins have been published. (nih.gov)
• Epigenetic alterations (or the "epigenome", when considering epigenetics on a genome-wide scale) include modifications to DNA, histone proteins that serve as a genome scaffold, and other factors including noncoding RNAs that collectively regulate the expression of genes without changing DNA sequence. (nih.gov)

Amino1

• Researchers believe that this abnormal amino acid sequence directs the protein into the nucleus of the cell, where it cannot form the strong network of intermediate filaments. (medlineplus.gov)

Alleles1

• 4. Phylogenetic history of hominoid DRB loci and alleles inferred from intron sequences. (nih.gov)

Genes4

• Van Tuinen, M., Sibley, C. & Hedges, S. B. Phylogeny and biogeography of ratite birds inferred from DNA sequences of the mitochondrial ribosomal genes. (nature.com)
• 5. HLA-DRB intron 1 sequences: implications for the evolution of HLA-DRB genes and haplotypes. (nih.gov)
• 9. Evolutionary relationship of HLA-DRB genes inferred from intron sequences. (nih.gov)
• 16. HLA class II "typing": direct sequencing of DRB, DQB, and DQA genes. (nih.gov)

Cohorts1

• Replication, fine-mapping, and sequencing studies are to be conducted in existing cohorts with defined phenotypes. (nih.gov)

Computational2

• How will a computational pipeline for analyzing raw sequencing data be established? (medscape.com)
• How will the tissue preparation, sequencing and computational pipeline for clinical use be analytically validated? (medscape.com)

Spencer2

• Publications for Richard Spencer, Ph.D., M.D. (nih.gov)
• Mulkern, R.V. and Spencer, R.G.S.: Diffusion Imaging with Paired CPMG Sequences. (nih.gov)

Reproducibility1

• Sequence Typing of used to confi rm reproducibility. (cdc.gov)

20181

• Last edit at 08/06/2018 09:25AM by rick reynolds. (nih.gov)

Human2

• Large tumor sequencing studies have demonstrated that human cancers of a given histologic type are often heterogeneous with regard to the mutations that drive their invasion and that the mutations present in individual tumors have major influences on the natural history of the tumor, and its responsiveness to therapy. (medscape.com)
• Large tumor-sequencing studies have established that human cancers of a given histologic type are often heterogeneous with regard to the mutations that drive their growth and invasion. (medscape.com)

Practice1

• We are excited to be working with PathoQuest to develop and offer the first Good Manufacturing Practice (GMP) accredited Integration Site Analysis test with nanopore sequencing. (businesswire.com)

Progress1

• Mr. Brepson continued, "This new Integration Site Analysis method, powered by Oxford Nanopore sequencing, will enable our customers to progress their biologics programmes with more certainty than ever before. (businesswire.com)

Studies1

• With this perspective, we will review some new types of clinical studies that are utilizing high-throughput DNA sequencing. (medscape.com)

Methods2

• Methods inherited from interface org.biojava.nbio.core.sequence.template. (biojava.org)
• Additionally, PathoQuest's ISA test is positioned to provide significant benefits (speed, accuracy, confidence in the results) compared to traditional sequencing methods. (businesswire.com)

Lung1

• Using DNA sequencing technique, we narrowed down a short CpG-rich segment (eight specific CpG sites in the CpG island within exon 1) of the TCF21 gene, which was unmethylated in normal lung epithelial cells but predominantly methylated in lung cancer cell lines. (nih.gov)

Gene1

• Differential methylation of a short CpG-rich sequence within exon 1 of TCF21 gene: a promising cancer biomarker assay. (nih.gov)

Study1

• A. The Sequenced Treatment Alternatives to Relieve Depression (STAR*D) Study, funded by the NIH National Institute of Mental Health, is a nationwide public health clinical trial. (nih.gov)

Time1

• How will sequencing be completed within a clinically relevant time frame? (medscape.com)

Results2

• How will the sequencing results be interpreted and related to treatment options? (medscape.com)
• How will sequencing results be collected and stored? (medscape.com)

Explore1

• Click molecule labels to explore molecular sequence information. (nih.gov)

Address1

• Questions to address in using high-throughput sequencing for oncology. (medscape.com)

Short1

• We specifically targeted this short CpG-rich sequence and developed a quantitative methylation-specific PCR assay suitable for high-throughput analysis. (nih.gov)

Field1

• Richard: Well, all infectious diseases have some common threads and I think once you get into the field of studying infectious diseases you can see similarities and sort of lessons that can be learned from all of these. (nih.gov)

Great1

• Richard made great use of the Wolfram Function Repository -a public resource of user-contributed Wolfram Language functions. (wolfram.com)

Applications1

• With over 20 peer reviewed publications on NGS applications in biosafety testing, PathoQuest is a leading expert in the application of Good Manufacturing Practices (GMP)-compliant next generation sequencing (NGS)-based biosafety testing. (businesswire.com)

Institute1

• Richard: I actually came to this institute as a postdoc on a project studying amyotrophic lateral sclerosis and post-polio syndrome. (nih.gov)

Work1

• Tried sequence as in deadeyes but does not work out any one have an illustration or a monkey see monkey do a 5 year old can understand. (modelshipworld.com)

Video1

• Video by Art of Problem Solving's Richard Rusczyk. (mathcounts.org)

Found1

• this arginine-rich region is not found in the normal keratin 10 protein. (medlineplus.gov)