TraPS-VarI
@TrapsVari
"It is more important to know what sort of patient has a disease, than to know what sort of disease a patient has." --r/TraPSVarI/ Join the Reddit Community
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Interested in discovering rare variants unique to an individual patient? ~~~~~~~TraPS-VarI WebApp is back Online~~~~~~ traps-vari.org/weblog/2018/03… #Genomics #variante #individualizedmedicine #raredisorders #geneticdisease #inbornerrors #Variant #mutation #DNA #TraPSVarI #mutations
~~Germline Variant-1 ::EGFR p.T790M::~~🧵 ⦿ Lung cancer patients often harbor actionable somatic mutations in exon 18-21 of #EGFR ⦿ After treatment many patients' tumors express therapy resisting EGFR p.T790M variant But this variant is not always tumor-specific #Lungcancer
~~List of Cancer Drugs, Targets & Indications~~ ---(as of Nov-2022)--- ⦿ Do you know how many licensed cancer drugs exist? ⦿ Here is the most complete list of #drugs, its #targets & cancer types vijaykr-cv.webs.com #CancerResearch #CancerAwareness
I just posted "Are you susceptible to cancer? How to figure this out?" on Reddit reddit.com/r/TraPSVarI/co…
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How to Merge Genotyping Data from Multiple Individuals? …s-individualized-biology.blogspot.com/2022/06/how-to… #genomes #nextgenerationsequencing #ngs #postdocs #phds #masters
I just posted "A piece of tumor from Cervix grown outside the body (Assn of American Medical Colleges, 1956)." on Reddit reddit.com/r/u_TraPS-VarI…
I just posted "The number of catalogued SNPs for human species rises again. Will it rise again??" on Reddit reddit.com/r/TraPSVarI/co…
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I just posted "Why do I smell bad like rotten fish or rotten eggs? Did I did inherit this condition?" on Reddit reddit.com/r/TraPSVarI/co…
I just posted "Germline genetic host factors as predictive biomarkers in immuno-oncology (IO))" on Reddit reddit.com/r/TraPSVarI/co…
Answer: How to run scipy.stats.gmean for rows contanining values less than 1 and zeros? stackoverflow.com/a/72732486/193… #python #datascience #Statistics
Answer: How to retain column with non-numerical objects after dividing all rows by the last row in pandas dataframe? stackoverflow.com/a/72729573/193… #python #dataframe #DataScience
Designing genotyping primers the easy way Do you want to genotype your cell line/tissue sample using Sanger #Sequencing / Restriction Analysis? dbSNP has a very convenient flanking region retrieval tool integrated. Here is an illustration on how to use it. #variation #mutation
Individuals with loss of function genetic variants of EVER1 or EVER2 multi-pass membrane proteins respond to human papillomavirus quite dramatically. @RareDiseases #raredisease #TreeMan "Tree Man" Syndrome: The Rare Genetic Disorder youthmedicaljournal.org/2020/10/13/tre… via @wordpressdotcom
Every human individual is is unique. In this post-genome era, it is time to consider the ‘Individualized therapy’ trials (n-of-1 trials). Particularly relevant for rare diseases and inborn errors Kimmelman shares his perspective @NatureMedicine nature.com/articles/s4159…
The Human Pangenome Project will create the human reference genome sequence representing different ethnic groups. A short film: vimeo.com/473532397 @massivesci @HumanPangenome @NHGRI_GSP #IndividualizedMedicine #PrecisionMedicine
In both mice and human, SNPs around the 'YXXM' proximal signalling motif of LTK, generating membrane protein variants:- LTK p. G750E LTK p. E763K cause B cell abnormalities similar to systemic lupus erythematosus. doi.org/10.1093/hmg/dd… #SLE #Lupus @LupusOrg @LupusResearch
Winter Semester Session begins from Nov 2 to Nov 4. "Individualized Approach to Cell Surface Proteins for Precision Medicine" univz.uni-goettingen.de/qisserver/rds?… #individualizedmedicine #precisionmedicine #personalizedmedicine #variants #drugdiscovery #COURSES #diagnosis #cancer #courses
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