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NCBI

@NCBI

Official account of the National Center for Biotechnology Information at

@NLM_NIH

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Bethesda, Maryland, USAncbi.nlm.nih.govتاریخ پیوستن فوریهٔ ۲۰۰۹

۸۲ دنبال‌شده

۵۸٫۸ هزار دنبال‌كننده

توییت‌های NCBI

NCBI

@NCBI

۲۴ اوت

ElasticBLAST is a new way to BLAST large numbers of queries, faster and on the cloud. Check out all the reasons you should use ElasticBLAST! #NCBIBLAST #CloudComputing 👉 ow.ly/oopl50KqJhh

Background image of a large cloud behind a man on a computer. Text says, " Why should you use ElasticBLAST?"

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NCBI

@NCBI

۲۴ اوت

You can learn more about this project and other works completed at our Beyond Phylogenies codeathon here: github.com/topics/beyond- 👏 Thanks for sharing and for your hard work at the event! #OpenScience

نقل‌توییت

Theo Sanderson

@theosanderson

· ۲۹ ژوئیه

Had a good week participating in the NCBI Beyond Phylogenies codeathon. One of the things our team achieved was to add links between tools used for viral phylogenetics You can now: - load @nextstrain trees in Taxonium - export out NS subtrees - get clade stats with @GenSpectrum

این رشته‌توییت نشان داده شود

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Updated #GeneReviews chapter on GLI3-related Pallister-Hall syndrome, characterized by anomalies ranging from polydactyly, asymptomatic bifid epiglottis, and hypothalamic hamartoma to laryngotracheal cleft with neonatal lethality: ow.ly/a4LU50KoCSV #rarediseases #genetics

ncbi.nlm.nih.gov

GLI3-Related Pallister-Hall Syndrome

NCBI

@NCBI

۲۴ اوت

Have you tried our new Foreign Contamination Screen (FCS) tool? It's a process that facilitates high-quality data submissions to GenBank. Learn more: ow.ly/EOb450KoEcj #NCBICGR

Circular background image of colors running together. Text reads: "Foreign Contamination Screen - New Tool - Submit high-quality data to GenBank"

Updated #GeneReviews chapter on citrullinemia type I, a spectrum that includes a neonatal acute form, a milder late-onset form, a form in which symptoms begin at pregnancy or post partum, & a form without symptoms or hyperammonemia: ow.ly/UPyB50KoCRl #rarediseases #genetics

ncbi.nlm.nih.gov

Citrullinemia Type I

Citrullinemia type I (CTLN1) presents as a spectrum that includes a neonatal acute form (the "classic" form), a milder late-onset form (the "non-classic" form), a form in which women have onset of...

NCBI

@NCBI

۲۲ اوت

The new Comparative Genome Viewer can help you easily identify genomic changes that may be significant to biology and evolution. Try it out and let us know what you think! Learn more about the visualization tool here: ow.ly/a7iZ50K4SNC #NCBICGR

CGV view of a region containing a relative inversion between two human assemblies. Text reads: "New Comparative Genome Viewer: Compare chromosome regions!"

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New #GeneReviews Resource for Genetics Professionals detailing genetic disorders associated with founder variants common in the Bedouin population: ow.ly/7KzS50KoCP8 #rarediseases #genetics

ncbi.nlm.nih.gov

Resources for Genetics Professionals — Genetic Disorders Associated with Founder Variants Common in...

A founder variant is a pathogenic variant observed at high frequency in a specific population due to the presence of the variant in a single ancestor or small number of ancestors. The presence of a...

NCBI

@NCBI

۱۹ اوت

Newly released CDC #poliovirus genome sequence from a NY patient now available in #GenBank! ow.ly/7zKW50KohNa

artists rendering of poliovirus particles

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NCBI

@NCBI

۱۸ اوت

GenBank release 251.0 (8/15/2022) is now available on the NCBI FTP site. This release has 19.55 trillion bases and 2.94 billion records! Read more 👉

ncbiinsights.ncbi.nlm.nih.gov

Announcing GenBank Release 251.0 - NCBI Insights

GenBank release 251.0 (8/15/2022) is now available on the NCBI FTP site. This release has 19.55 trillion bases and 2.94 billion records. The current release has 239,915,786 traditional records...

NCBI بازتوییت کرد

National Library of Medicine

@NLM_NIH

۱۷ اوت

Learn more about the Diversity in #DataScience and #Informatics (DDSI) Internship, hosted by the NLM Intramural Research Program: nlm.nih.gov/research/DDSI.

نقل‌توییت

· ۱۷ اوت

Meet the next generation of leaders advancing #DataScience & #Informatics at @NLM_NIH! Today's guest post by Dr. Virginia Meyer spotlights four interns from diverse backgrounds working w/ principal investigators across the NLM Intramural Research Program. nlmdirector.nlm.nih.gov/2022/08/17/mee

NCBI بازتوییت کرد

National Library of Medicine

@NLM_NIH

۱۷ اوت

NLM is one of the U.S. federal agencies responding to the #monkeypox public health emergency w/ scholarly publishing resources. We are working w/ publishers that submit to PubMed Central to make certain journal articles freely available, boosting access to research & results.

نقل‌توییت

White House Office of Science & Technology Policy

@WHOSTP

· ۱۵ اوت

Swift access to #monkeypox research & data is imperative to how we stop this outbreak & ultimately save lives. We are pleased to report that a number of scholarly publishers & organizations have taken actions to make monkeypox information more accessible. whitehouse.gov/ostp/news-upda

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NCBI

@NCBI

۱۷ اوت

Want to learn how to use NCBI's Foreign Contamination Screen? Join us for a short webinar September 7th! #SciEd #GenomeSequencing 👉 ow.ly/Lhi850Kliau

ncbiinsights.ncbi.nlm.nih.gov

Using NCBI Foreign Contamination Screen to Remove Contaminants from Genome Assemblies - NCBI...

Learn how to use the new NCBI FCS tool suite to identify and remove contaminants from your genome assemblies.

Without more diverse genomic datasets, it will be difficult to ensure that all communities equally benefit from genomic medicine. For example, scientists find that genomic variants influencing common, complex diseases vary greatly in their frequency across different populations.

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این رشته‌توییت نشان داده شود

NCBI

@NCBI

۱۱ اوت

Publication and sequence data from the recent zoonotic #henipavirus (#langya) outbreak now available from NCBI! Publication: ow.ly/9VmI50Ki9Hx Genome seqs: ow.ly/Aku550Ki9Iz Gene seqs: ow.ly/4X0350Ki9Jl

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NCBI

@NCBI

۱۰ اوت

A BIG thank you to the participants of our codeathon, Investigating Accurate & Equitable Representation in PubMed Search Results. We had a wonderful time learning together! Interested in getting involved in NCBI Codeathons? Keep an eye on this page! 👇 ow.ly/zWe450KgfLl

"Thank you to our codeathon contributors" overlaid on a blue image of a person typing and data components.

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NCBI

@NCBI

۱۰ اوت

New links and annotations on Conserved Domain Search results (PubMed, Go Terms, EC numbers, SPARCLE Domain Architecture! ow.ly/3NwS50KgQ0C #NCBICGR

ncbiinsights.ncbi.nlm.nih.gov

Announcing new links and annotations on Conserved Domain Search results! - NCBI Insights

Conserved Domain Search (CD Search) results now show domain architecture information and other annotations that further characterize predicted domain and protein function. These include links to...

NCBI

@NCBI

۸ اوت

With the Comparative Genome Viewer you can compare two assemblies to see differences in genomic sequence and structure. Check out our new visualization tool! ow.ly/6aTK50K4S7W #NCBICGR

Background is the CGV chromosome-level view comparing chromosomes and text reads: "Compare chromosomes! New Comparative Genome Viewer"

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NCBI

@NCBI

۸ اوت

Thanks for joining our workshop! We love hearing from the community about the work you are doing. 👏 Stay tuned for future outreach events: ow.ly/gfyR50Kfer8

نقل‌توییت

raphael mensah

@ralphmends

· ۶ اوت

Delighted to have completed this amazing NCBI workshop on Introduction to Pathogen Data fantastically facilitated by Dr. Rana Morris and ⁦@NCBI⁩ I am enjoying developing my knowledge in computational biology and bioinformatics to help further my understanding of the field.

Updated #GeneReviews chapter on epidermolysis bullosa simplex (EBS), characterized by fragility of the skin (and mucosal epithelia in some instances) that results in non-scarring blisters and erosions caused by minor mechanical trauma: ow.ly/VSwP50Keemv #rarediseases

ncbi.nlm.nih.gov

Epidermolysis Bullosa Simplex

Epidermolysis bullosa simplex (EBS) is characterized by fragility of the skin (and mucosal epithelia in some instances) that results in non-scarring blisters and erosions caused by minor mechanical...

NCBI

@NCBI

۸ اوت

There are twenty-six new NCBI annotations in RefSeq for snow leopard, dingo (pictured), brown dog tick, malaria mosquito, rock ptarmigan, marmot, loggerhead turtle, and more: ow.ly/7Fwu50KeROQ #NCBICGR

ncbiinsights.ncbi.nlm.nih.gov

New annotations in RefSeq - NCBI Insights

In June and July, the NCBI Eukaryotic Genome Annotation Pipeline released twenty-six new annotations in RefSeq for the following organisms: Anopheles coluzzii (mosquito) Anopheles funestus (African...

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NCBI بازتوییت کرد

Joint Genome Institute

, Tom Madden

, and

when you register to attend our #JGI2022

@jgi

Annual Meeting at usermeeting.jgi.doe.gov.

Updated #GeneReviws chapter on thiamine-responsive megaloblastic anemia syndrome (TRMA), characterized by megaloblastic anemia, progressive sensorineural hearing loss, and diabetes mellitus: ow.ly/HjV350K8ASk #raredisease #genetics #health

ncbi.nlm.nih.gov

Thiamine-Responsive Megaloblastic Anemia Syndrome

Thiamine-responsive megaloblastic anemia syndrome (TRMA) is characterized by megaloblastic anemia, progressive sensorineural hearing loss, and diabetes mellitus. Onset of megaloblastic anemia occurs...

#NIH supports a coordinated approach to swiftly sharing #monkeypox research results including registering and reporting trial results in clinicaltrials.gov and submitting journal articles in PubMed Central.

نقل‌توییت

White House Office of Science & Technology Policy

@WHOSTP

· ۴ اوت

To accelerate efforts to mitigate the #Monkeypox outbreak, @WHOSTP coordinated with 19 allies and partners in calling on publishers to immediately allow access to relevant research and data. whitehouse.gov/ostp/news-upda

این رشته‌توییت نشان داده شود

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Updated #GeneReviws chapter on MPPH syndrome, a developmental brain disorder characterized by megalencephaly (brain overgrowth) with the cortical malformation bilateral perisylvian polymicrogyria: ow.ly/GiaC50K8Afj #raredisease #genetics #health

ncbi.nlm.nih.gov

MPPH Syndrome

MPPH (megalencephaly-postaxial polydactyly-polymicrogyria-hydrocephalus) syndrome is a developmental brain disorder characterized by megalencephaly (brain overgrowth) with the cortical malformation...

Updated #GeneReviews chapter on Kaufman oculocerebrofacial syndrome (KOS), which is characterized by developmental delay, severe intellectual disability, and distinctive craniofacial features: ow.ly/84l850K8zzz #raredisease #genetics #health

ncbi.nlm.nih.gov

Kaufman Oculocerebrofacial Syndrome

Kaufman oculocerebrofacial syndrome (KOS) is characterized by developmental delay, severe intellectual disability, and distinctive craniofacial features. Most affected children have prenatal-onset...

NCBI بازتوییت کرد

National Library of Medicine

@NLM_NIH

۲ اوت

📣 The Laboratory of Structural Bioinformatics at NLM has two open postdoctoral positions: • Computational Biology/Structural Bioinformatics: loom.ly/7_DSKYY • Structural Biology/Biophysics: loom.ly/SJsYUnE Positions open until filled.

@IRPatNIH

@NIH_OITE

این رشته‌توییت نشان داده شود

NCBI

@NCBI

۲ اوت

We have added several exciting features to our tool iCn3D! Learn more here! 👇 ow.ly/EemA50K8Vf2 #AlphaFold #VR #AR #3DViz #StructuralBio

Person using a VR headset in the dark + text that reads, "Expanded analysis of alphafold structures, VR and AR in iCn3D"

New #GeneReviews chapter on GRIN2D-related developmental and epileptic encephalopathy (GRIN2D-related DEE), characterized by developmental delay or intellectual disability, epilepsy, and autism spectrum disorder among other features: ow.ly/JhAE50K8yZQ #raredisease #genetics

ncbi.nlm.nih.gov

NCBI بازتوییت کرد

National Library of Medicine

@NLM_NIH

۱ اوت

NLM is pleased to invite all who are interested to the virtual Lindberg-King Lecture & Scientific Symposium, "Science, Society, and the Legacy of Donald A.B. Lindberg, M.D.," on Thurs, 9/1 at 9:00 a.m. ET. Register to attend:

eventbrite.com

2022 NLM Lindberg-King Lecture & Scientific Symposium

2022 Lindberg-King Lecture and Scientific Symposium: Science, Society, and the Legacy of Donald A.B. Lindberg, M.D.

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این رشته‌توییت نشان داده شود

NCBI بازتوییت کرد

National Library of Medicine

@NLM_NIH

۲۸ ژوئیه

📣 The

@jiang_bioinfo

lab at NLM invites qualified applications for postdoctoral research positions in two areas: • Bioinformatics/#DataScience: loom.ly/CRL4jwM • #MachineLearning/Statistics: loom.ly/Ld-5q24 Positions open until filled.

@IRPatNIH

@NIH_OITE

این رشته‌توییت نشان داده شود

NCBI

@NCBI

۲۸ ژوئیه

Want to submit high-quality data to #GenBank? Check out our new Foreign Contamination Screen (FCS) tool, a quality assurance process, that you can now run yourself! #NCBICGR ow.ly/zQXN50K6t2T

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NCBI

@NCBI

۲۷ ژوئیه

Announcing the #NCBIDatasets #SARSCoV2 taxonomy page to access genomes, proteins, information about SARS-CoV-2, and connections to related NCBI pages!

ncbiinsights.ncbi.nlm.nih.gov

Announcing the NCBI Datasets SARS-CoV-2 taxonomy page - NCBI Insights

Need SARS-CoV-2 assembled genome sequences or specific SARS-CoV-2 protein sequences? You can find them on the new SARS-CoV-2 taxonomy page brought to you by NCBI Datasets. The NCBI Datasets SARS-Co...

NCBI

@NCBI

۲۷ ژوئیه

Learn how to find, browse, and download NCBI genome data more easily than ever with NLM's #NCBIDatasets! Join us for a guided tour of our genome and taxonomy pages, and our all-new genome table: ow.ly/m1HW50K4xMb. #NCBICGR

youtube.com

Easy Access to Data with NLM's NCBI Datasets!

NCBI Datasets is a developing resource that lets you easily find, browse and download data at NCBI. In this video, we'll highlight some new web pages for fin...

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New #GeneReviews chapter on carnitine-acylcarnitine translocase (CACT) deficiency, which causes a defect in mitochondrial long-chain fatty acid β-oxidation, with variable clinical severity:

ncbi.nlm.nih.gov

Carnitine-Acylcarnitine Translocase Deficiency

Carnitine-acylcarnitine translocase (CACT) is a critical component of the carnitine shuttle, which facilitates the transfer of long-chain fatty acylcarnitines across the inner mitochondrial membrane....

NCBI

@NCBI

۲۲ ژوئیه

Quickly compare eukaryotic genomes with our new Comparative Genome Viewer! Learn more about this easy-to-use visualization tool: ow.ly/wv2F50K1zVu #NCBICGR

Background is a CGV full genome comparison view of two assemblies. Text says: New Comparative Genome Viewer, Compare full genome assemblies!

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نقل‌توییت

· ۱۴ ژوئیه

Try out the latest BLAST ClusteredNR database results. Now with in-cluster analyses! ow.ly/e0gX50JW0zu

NCBI

@NCBI

۲۰ ژوئیه

NCBI's Nuala O’Leary, PhD, will demo Datasets TODAY at 10:20 AM CDT. Don't miss it! More information: ow.ly/24GJ50JQIlP #NCBICGR #UseGalaxy2022

NCBI

@NCBI

۱۹ ژوئیه

We want to help you get the most out of NCBI tools and resources! Check out our support page and browse our health topics, including BLAST, Genes & Genomes, Submitting Data, and more! ow.ly/SpPI50JuJg8

graphic of NLM support center page with various health topics including Health, Literature, BLAST and more.,

NCBI

@NCBI

۱۹ ژوئیه

Join Nuala O’Leary, PhD, TODAY for her talk about Datasets, a new resource that makes it easier to access NCBI sequence data. Learn more: ow.ly/bHpg50JQHAy #NCBICGR #UseGalaxy2022

head shot of Dr. O'Leary and information about her talk at GCC2022

NCBI

@NCBI

۱۹ ژوئیه

RefSeq Release 213 is now available! This full release incorporates genomic, transcript, and protein data available as of July 11, 2022. Learn more:

ncbiinsights.ncbi.nlm.nih.gov

RefSeq Release 213 - NCBI Insights

RefSeq Release 213 is now available online, from the FTP site and through NCBI’s Entrez programming utilities, E-utilities. This full release incorporates genomic, transcript, and protein data...