Updated #GeneReviews chapter on APC-associated polyposis conditions, which include (classic or attenuated) familial adenomatous polyposis (FAP) and gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): ow.ly/FT3850J8XVl #rarediseases #genetics #health
NCBI’s Tweets
Applications for our virtual workshop, "An Introduction to NCBI Cloud Computing for Virologists" are OPEN NOW! More info here 👇
loom.ly/EXkCN60
#CloudComputing #SciEd #GradChat #Bioinformatics
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New #GeneReviews chapter on PPP2R1A-related neurodevelopmental disorder, characterized by hypotonia, developmental delay, seizures, ADHD & other behavioral problems, feeding & swallowing issues, and dysmorphic head & facial features: ow.ly/hOr550J8Xw1 #rarediseases #health
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Updated #GeneReviews chapter on NOTCH3-related lateral meningocele syndrome, characterized by multiple lateral spinal meningoceles distinctive facial features, joint hyperextensibility, hypotonia, and other anomalies: ow.ly/Ssct50J2THq #rarediseases #genetics #health
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Updated #GeneReviews chapter on hereditary folate malabsorption, characterized by folate deficiency due to impaired intestinal folate absorption and impaired folate transport into the central nervous system: ow.ly/KbVb50J2T24 #rarediseases #genetics #health
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💻 New #Codeathon Opportunity! We are teaming up with the National Institute of Allergy and Infectious Diseases to host a Beyond Phylogenies Visualizations Codeathon. Apply today! 👇
loom.ly/sBxKaqo
#Bioinformatics #CodingLife #Networking
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RefSeq Release 212 is available and contains the first new annotation of human in four years! It also contains new annotations for 29 species, including: gray squirrel, American grasshopper, and fishing cat. Read more:
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Apply to our virtual workshop, "Using NCBI’s Primer-BLAST to Design & Analyze PCR Primers" by May 23rd! Learn more here: loom.ly/xwexYbY
#SciEd #BLAST #Bioinformatics #PrimerDesign
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Join us THIS week at the #BoG22 (May 10-14)! Learn how we support eukaryotic genomes research when Valerie Schneider, PhD, presents her poster, The NIH Comparative Genomics Resource: Amplifying the biology of genomes. Register for virtual participation: ow.ly/efIi50IXjTG
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Submit your science for an opportunity to present it to colleagues at #ASHG22! Abstracts are due June 9: bit.ly/3ym4N6K
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Recognize #NationalNursesWeek by reading on the NLM Bookshelf reports about their role in patient safety and evidence-based healthcare: ow.ly/9gSo50IZm31
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The Bio-IT World 2022 Hackathon starts TODAY! Join NCBI to learn about and work with data from our ALFA project: Visualization of NCBI ALFA Variants. Read about the project and find registration information here:
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Updated #GeneReviews chapter on MBD5 haploinsufficiency, a neurodevelopmental disorder characterized by developmental delay, intellectual disability, severe speech impairment, seizures, sleep disturbances, and abnormal behaviors. #rarediseases #genetics
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Come see us TODAY at the Bio-IT World Conference and Expo and learn more about ElasticBLAST! Look for poster P11. #ElasticBLAST #CloudComputing #NCBIBLAST #BioIT22
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Reminder to register for the Bio-IT World 2022 Hackathon coming up THIS week (May 4-5, 2022)! Join NCBI to learn about and work with data from our ALFA project. More information and registration links can be found here:
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NCBI is making it easy to run BLAST on the cloud! #ElasticBLAST #CloudComputing #NCBIBLAST #BioIT22 ow.ly/eW3X50ITIxl
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Check out 's feature on NCBI's own Dr. L. Aravind Iyer! His research aims to uncover evolutionary patterns of DNA and RNA.
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Updated #GeneReviews chapter on PRICKLE1-related disorders, which typically presents with progressive myoclonus epilepsy with ataxia: ow.ly/jJ5L50IRLjo #rarediseases #genetics #health
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Logging into your My NCBI account is now easier, faster and more secure! As of June 2022, you will be required to login using a 3rd-party option. Find more information about new login requirements here:
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Updated #GeneReviews chapter on neurofibromatosis 1, a multisystem disorder characterized by multiple café au lait macules, intertriginous freckling, multiple cutaneous neurofibromas, and learning disability or behavior problems: ow.ly/cbrQ50IRLf9 #rarediseases #genetics
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Updated #GeneReviews chapter on chronic granulomatous disease, a primary immunodeficiency disorder of phagocytes resulting from impaired killing of bacteria and fungi: ow.ly/aR2g50IRKXF #rarediseases #genetics #health
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📢One month until we deliver this exciting, virtual workshop! Apply today! #GradChat #Bioinformatics #ScienceTwitter #NCBI #Workshops
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The makeblastdb program in BLAST+ 2.2.13 produces database metadata in #JSON format! loom.ly/Ny7gHb4
#NCBIBLAST
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Updated #GeneReviews chapter on Schimke immunoosseous dysplasia (SIOD), characterized by spondyloepiphyseal dysplasia (SED) resulting in short stature, nephropathy, and T-cell deficiency: loom.ly/OUqPUFM #rarediseases #genetics #health
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