Skip to main content

Rohit, Week 2.5 at the Berkeley Deep Drive Lab

After I learned the basics of how to use and write code in Python my doctorate student Mr. Long Xin gave me a simple task so that I could learn how to write code to help with data analysis of raw data using python. My task was to replicate and manipulate the data in order to calculate the average velocity of a vehicle as it passed through an intersection. The data was captured by an array of cameras on a high rise building located right next to the intersection. The raw data may seem imposing at first as it look like a string of random numbers, but in reality there is a specific way to decode and understand what the actual data means. For example the first number in each entry is the individual vehicle id for example 284 refers to a single vehicle and all entry's beginning with 284 refer to the values recorded for that unique vehicle. The rest of the values correspond to other terms such as velocity over a tenth of a second etc. This assignment helped me learn how to apply python in order to simplify and calculate data easily from hundreds of individual entries without having to manually enter all the individual values of velocity and then adding them to calculate the mean  velocity over the recorded period.

In terms of activities outside of the lab living in Berkeley with Alan has been fun, our apartment building has a Trader Joe's on the first floor, which means groceries are not an issue. We also have a washer and dryer in our apartment, which is also another key convenience aspect. Over the weekend we went to San Francisco and explored the city. 

Comments

Post a Comment

Popular posts from this blog

Kylie Heering, Week 2 at the Goldstein Lab

We started off our week with a congratulatory acai bowl trip to celebrate Preston’s acceptance into a training grant program. Acai bowls in California top Playa Bowls (no question about it). From what I can tell, its a pretty huge honor to be recognized by this grant, but he’s really humble about it. On Monday, Preston and I decided that testing antibodies that have never been tested on prostate epithelial cells before would be a good objective for my first Western blot on my own. We needed to probe for ASCT2, a glutamine transporter, and GLS in order to determine if their corresponding antibodies are functional. Antibodies are crucial for Western blots because they bind to the protein of interest (POI), allowing for us to qualify its expression after imaging. As such, Preston wanted to make sure they worked by probing for ASCT2 and GLS on three different cell lines. Cell lines are commercially purchased human cells that have been immortalized (modified to grow indefinitely) by telome...

Alan - First Week at UCSF

Hi Everyone! After arriving in San Francisco last Sunday, I spent this past week settling into the downtown Berkeley apartment that I’ll be sharing with Rohit for the next couple of months, as well as learning my way around the Roy lab at UCSF. First day at the lab was really exciting. Here are a couple pictures of the Mission Bay campus, which was completed just a few years ago. Everything is super new and modern, and there’s still construction for other buildings going on around the campus. Most of the people who work at the Mission Bay campus are either professional researchers or doctors/nurses for the nearby hospital. The graduate students take most of their classes at the original Parnassus campus (where Maya is). I work in Byers Hall, which is connected to Genentech Hall and a short walk down the block from the shuttle stop. There are three other volunteers working for the Roy lab this summer – Kimmai, David, and Pujita, who are all undergrad college students...

Jaewon Oh - Week 7 and 8

Finally done here with my experience and I wish I had more time keep researching so that I have something a little more "finalised" to present. But I guess that's what past EXP kids meant when they said that 8 weeks of research is not enough and I'll have to work with what I've got. To solve the problem of not having enough data points, we used the online TCGA database for raw data that would be used to calculate mutation rates. Mutation rates were calculated through an R coding script that Dr. Cannataro had made. Because the mutation rates were tumor specific, we had to change the proportions that were obtained from the IARC database using data from another database called cBioPortal. Basically we had to multiply the number of times a certain variant was seen in the IARC database by the percentage of tumors that have a tp53 mutation, because our mutation rates are calculated across all tumors in specific cancers (confusing, I know). After graphing the mutatio...