![]() u/ChanceAnt 's screenshot makes me think that an internal error (either human error or system error) made the SAT/ACT item show as awaiting and that the new dates are someone cleaning them up manually. I suppose they could be doing that as some sort of pre-review test score verification, but that seems unlikely to me because it would be really tedious for little benefit and a lot of confusion. The only way to change the received date, that I'm aware of, is to change it manually. This is why many institutions show the specific test dates received below the checklist. Stanford could totally have something more custom set up, but speaking generally, the date checklist items are received is static and won't change even if a new item of the same type is received. I don't have any knowledge of Stanford's internal review processes, but I do know they use Slate and I know a fair amount about Slate. I'll make an update post in a few weeks (before decisions) to see whether it holds up. The most sensical theory seems to be the one posted by u/Ut-Mis_is_great (see top comment below). UPDATE: Okay, so it's been a few hours since I posted this, and the results seem to be similar to the CC (blegh) thread. I found it kinda strange, since it hasn't happened with any of my other portals. TL DR If you login to the Stanford portal, the "date received" for (self-reported) SAT/ACT scores changed for some people recently. Kinda strange that it would update on the portal though.Īnyway, as I continue procrastinating on work, I was interested to hearing your theories about this, thought it might make a fun little thread on here. Personally, I think it just means your application has been reviewed. Obviously, with it being CC, people think it has to do with whether you're accepted or rejected. Previously (if self-reported), it would have just stated the same day as the application. Essentially, it says that if you log into the Stanford portal, some people see that the date when the SAT/ACT was received changed quite recently (some people saw it change to late Feb, others to early March). People on there were discussing something pretty interesting. Yesterday, I was lurking on the Stanford RD 2023 Applicants thread, just to see what's up, while procrastinating on decisions. To learn more about the functionalities, watch the tutorial videos: Understanding the Dashboard Searching and Browsing Identifying Molecular Interactions.So, I think most people on here can agree that CollegeConfidential is a pretty toxic site. ![]() It allows easy navigation to computational and non-computational biologists. The CTD 2 Dashboard is an interactive web database that hosts positive results and allows users to connect targets, biomarkers, and modulators with evidence to support the validation. Not all projects on the Data Portal have links to Dashboard submissions as the follow-up studies of the primary screening may be in progress or not yet pursued. ![]() The Data Portal contains a wealth of information: brief descriptions of research projects, experimental approaches, links to download raw/primary data, and links to associated validated studies in the Dashboard. Examples of data types on the Data Portal include chemical genetic screens (small-molecules, natural products) genome-wide gain-of-function (cDNA expression libraries, CRISPRa) genome-wide loss-of-function (siRNA, shRNA, CRISPR/Cas9, CRISPRi) and protein-protein interactions, etc. The CTD 2 Data Portal provides access to raw/analyzed primary data generated from different types of experimental and computational approaches. The CTD 2 is a “ community resource project” and Network members release their data to the Data Portal and Dashboard so that other investigators can utilize it and thereby maximize the impact of the findings.ĭata generated by CTD 2 Network teams can be accessed through the Data Portal and the Dashboard. The Cancer Target Discovery and Development (CTD 2) Network aims to understand the mechanisms of tumor progression, heterogeneity, and drug resistance and applies the knowledge for the development of efficient strategies to identify optimal combinations of small-molecules or immunotherapy with small molecules.
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