Difference between revisions of "Team:IISER-Pune-India/Collaborations"

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<p>We collaborated with other iGEM teams in three different ways-
 
<p>We collaborated with other iGEM teams in three different ways-
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<li>Wet lab work for team IISc Bangalore : Data collection for machine learning</li>
 
<li>Wet lab work for team IISc Bangalore : Data collection for machine learning</li>
 
<li>All India iGEM Meet-up at IISER Pune<li/>
 
<li>All India iGEM Meet-up at IISER Pune<li/>

Revision as of 19:10, 28 October 2017

Medal Criteria

Collaborations

“Many ideas grow better when transplanted into another mind than the one where they sprang up.”-Oliver Wendell Holmes

We collaborated with other iGEM teams in three different ways-

  1. Wet lab work for team IISc Bangalore : Data collection for machine learning
  2. All India iGEM Meet-up at IISER Pune
  3. iGEM groups on social media and Whatsapp

IISc Bangalore Collaboration

Their team was trying to build a precise and time effective way to measure the cell count of yeast cultures. They wanted to collect a huge amount of data to train a ​machine learning algorithm that they had designed for counting these cells. Collecting such huge amount of data means growing hundreds of yeast cultures,collecting samples every hour and then imaging it under the microscope on hemocytometer. It is a tedious task to be done alone by a team. Thus, with this collaboration our team was expected to generate images for the algorithm to analyze by monitoring one growth curve for Saccharomyces cerevisiae.

An introduction to machine learning that team IISc Bangalore has designed can be found here

We were asked to follow the following protocol-

Mentioned below is the protocol that we followed in which we have made certain modifications to the above protocol-

DAY 1: Primary Inoculum

  1. In a sterile hood, inoculate a colony of ​S.cerevisiae ​in ​5 mL ​of ​YPD/YPAD​( 2 replicates). (Since we didn’t have the lab strain of ​S.cerevisiae and this experiment needed only quantitative data for the machine learning algorithm ,we used common baker’s yeast for the culture.) Comment-This was something exciting!
  2. Incubate the culture at ​30⁰C,​​overnight​, at ​180 RPM​.

DAY 2: The Growth Curves

a) MAKING THE SECONDARY INOCULUM

  1. Add 2.5 mL of primary inoculum to 247.5 mL of YPD/YPAD in a 1L flask in sterile environment.
  2. Swirl flask gently.
  3. Take​‘0’th time point ​sample for both replicates and store it at 4 degrees.
  4. Seal mouth of flask with a cotton plug, incubate at ​30⁰C ​and ​180 RPM​.
  5. Take samples ​every one hour ​for the growth curve for ​16 hours​.(Comment-We literally spent the entire night in the lab)

b) TAKING MEASUREMENTS

Here are some suggestions for projects you could work on with other teams: