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    * Latest "Sequence-tagged-site-(STS)" in the News * 

 

 
Novel Y-chromosomal microdeletions associated with non-obstructive azoospermia uncovered by high throughput sequencing of sequence-tagged sites (STSs)  Nature.com

Y-chromosomal microdeletion (YCM) serves as an important genetic factor in non-obstructive azoospermia (NOA). Multiplex polymerase chain reaction (PCR) is ...

Molecular mapping: Genetic and physical maps.  Science 2.0

Genome:A genome is all the DNA in anorganism, including its genes.• Comparative Sequence Sizes (Bases)• Escherichia coli(bacterium) genome 4.6 Million.

Whole-Genome Sequence Analysis of Streptococcus pneumoniae Strains That Cause Hospital-Acquired Pneumonia Infections  Journal of Clinical Microbiology

Streptococcus pneumoniae colonizes the nasopharyngeal mucus in healthy individuals and can cause otitis media, pneumonia, and invasive pneumococcal ...

Defining and Evaluating a Core Genome Multilocus Sequence Typing Scheme for Genome-Wide Typing of Clostridium difficile  Journal of Clinical Microbiology

Clostridium difficile, recently renamed Clostridioides difficile, is the most common cause of antibiotic-associated nosocomial gastrointestinal infections worldwide ...

Whole-Genome Sequencing of Recent Listeria monocytogenes Isolates from Germany Reveals Population Structure and Disease Clusters  Journal of Clinical Microbiology

Listeria monocytogenes causes foodborne outbreaks with high mortality. For improvement of outbreak cluster detection, the German consiliary laboratory for ...

Inhibition of FAST-1 Molecule May Have Therapeutic Potential in Friedreich’s Ataxia, Study Confirms  Friedreich's Ataxia News

A study supports the hypothesis that inhibition of FAST-1, a naturally produced RNA molecule, may have potential for the treatment of Friedreich's ataxia.

Copy number variation and microdeletions of the Y chromosome linked genes and loci across different categories of Indian infertile males  Nature.com

We analyzed 34 azoospermic (AZ), 43 oligospermic (OS), and 40 infertile males with normal spermiogram (INS) together with 55 normal fertile males (NFM) from ...

Validation of Whole-Genome Sequencing for Identification and Characterization of Shiga Toxin-Producing Escherichia coli To Produce Standardized Data To Enable Data Sharing  Journal of Clinical Microbiology

Whole-genome sequencing (WGS) is rapidly becoming the method of choice for outbreak investigations and public health surveillance of microbial pathogens.

Large Interruptions in GAA Repeats are Rare Among FA Patients, Study Finds  Friedreich's Ataxia News

Large interruptions of GAA repeats in the frataxin (FXN) gene are very rare among patients with Friedreich's ataxia (FA), a study has found. However, when these ...

Ultrafast manipulation of mirror domain walls in a charge density wave  Science Advances

Domain walls (DWs) are singularities in an ordered medium that often host exotic phenomena such as charge ordering, insulator-metal transition, ...

Case Report Describes Early FA Onset in Boy with Rare Gene Mutation  Friedreich's Ataxia News

A new case report describes a 7-year-old boy with Friedreich's ataxia (FA) who has a particularly early age of disease onset and an extremely rare type of ...

DNA Repair Protein Could Be Key to Understanding FA Progression, Study Suggests  Friedreich's Ataxia News

Read about the role of the MLH3 protein in Friedreich's ataxia and its potential as a therapeutic target to prevent GAA repeat expansion and modify the disease's ...

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     Internet Search Results 

STS - Wikipedia
This disambiguation page lists articles associated with the title STS. If an internal link led you here, you may wish to change the link to point directly to the intended article.

What does STS stand for? - Abbreviations.com
Looking for the definition of STS? Find out what is the full meaning of STS on Abbreviations.com! 'Sequence Tagged Site' is one option -- get in to view more @ The Web's largest and most authoritative acronyms and abbreviations resource.

STS — Wikipédia
Sigles de 2 caractères Sigles de 3 caractères Sigles de 4 caractères Sigles de 5 caractères Sigles de 6 caractères Sigles de 7 caractères Sigles de 8 caractères

Information on Anxiety and Anxiety Disorder | HealthCentral
Expert information and cutting-edge research on different kinds of anxiety disorders, including obsessive-compulsive disorder and post-traumatic stress disorder, with inspiring testimonials from ...

FASTA/SSEARCH/GGSEARCH/GLSEARCH < Sequence Similarity ...
FASTA (pronounced FAST-AYE) is a suite of programs for searching nucleotide or protein databases with a query sequence. FASTA itself performs a local heuristic search of a protein or nucleotide database for a query of the same type. FASTX and FASTY translate a nucleotide query for searching a protein database. TFASTX and TFASTY translate a nucleotide database to be searched with a protein query.

Contig - Wikipedia
A contig (from contiguous) is a set of overlapping DNA segments that together represent a consensus region of DNA. In bottom-up sequencing projects, a contig refers to overlapping sequence data (reads); in top-down sequencing projects, contig refers to the overlapping clones that form a physical map of the genome that is used to guide sequencing and assembly.

NCBI BLAST < Sequence Similarity Searching < EMBL-EBI
BLAST stands for Basic Local Alignment Search Tool.The emphasis of this tool is to find regions of sequence similarity, which will yield functional and evolutionary clues about the structure and function of your sequence.

What's a Genome?
What's a Genome? What's a Chromosome? What's a Gene? What's DNA? What's Genome Sequencing? What's a genome map? What does a genome map look like? What is the difference between a genome map and a genome sequence?

The Sleep Disorder Canine Narcolepsy Is Caused by a ...
The Sleep Disorder Canine Narcolepsy Is Caused by a Mutation in the Hypocretin (Orexin) Receptor 2 Gene

Mappatura dei genomi, Giovanni Paolella « Biotecnologie ...
Il linkage. Le leggi di Mendel si applicano correttamente a geni localizzati su cromosomi diversi. Geni localizzati sullo stesso cromosoma tendono invece a essere ereditati insieme: il fenomeno è noto come linkage.. In realtà un linkage completo si osserva solo per geni molto vicini, mentre geni progressivamente più lontani mostrano il fenomeno in grado via via decrescente.

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