MiRPathDB Week 5

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Lab Notebook

Planning the Project

As homework partner, Quinn Lanners and John Lopez worked together to analyze the miRPathDB database by following the template laid out on the week 5 assignment page.

To start this weeks assignment, we selected a database from one of the ones on the Nucleic Acids Research Database Issue Table of Contents 2017. After we had selected a database, and it was approved by Dr. Dahlquist, we began work on the assignment.

To make better use of our time, we decided on Thursday to break up the questions between ourselves. Then we could work separately on our own time to find the answers before coming together to put all of the information into a PowerPoint presentation. We decided that John would handle the questions "General Utility" questions of the database, while Quinn would handle the "Scientific Quality" questions of the database. As for the "General Information", which we figured would be easier to determine, we decided to answer those questions each individually as we looked into our specific part. Since the database research was broken up in this manner, the following section of the electronic journal is comprised of two separate accounts from each of us about how we retrieved the answers to our assigned questions.

Questions

  • General Information: (answered on October 1st by John)
  1. The name of the database is miRPathDB Source: (https://mpd.bioinf.uni-sb.de/overview.html)
  2. Two answers:
    1. This database contains mainly miRNA molecules and the different pathways you can find said molecule in. Source: (https://mpd.bioinf.uni-sb.de/about.html)
    2. Since the data for the database is collected through several previously-established databases, it is considered a secondary database. It is curated constructed using computer programs, electronically. We know it was made using in-house staff because all of the researchers’ names are listed. Source: (https://mpd.bioinf.uni-sb.de/about.html)
  3. It would appear that the Center for Bioinformatics at Saarland University maintains the database. They are a large, public research university. Sources: (http://www.uni-saarland.de/en/info/university/about.html), (https://mpd.bioinf.uni-sb.de/about.html)
  4. Only the funding for keeping it open access was displayed, and tis came from Saarland University. ‘’’Source:’’’ (https://academic.oup.com/nar/article/45/D1/D90/2290890/miRPathDB-a-new-dictionary-on-microRNAs-and-target)

I aimed to answer the following questions regarding our database:

  • Scientific quality of the database: (answered on October 1st by Quinn)

In order to answer these questions I read the article covering the miRPathDB from the Nucleic Acids Research and by analyzing the actual miRPathDB website.

  • General Utility: (answered on October 1st by John)
  1. Whenever a search is performed for an miRNA molecule, the database provides a link to that molecule from the following sites: (http://www.mirbase.org/). It also directs you to a link that tells you what tissue that molecule might be located in using the following site: (https://ccb-web.cs.uni-saarland.de/tissueatlas/patterns). NOTE: It will link you to these databases whether or not you search a mouse or human miRNA. Sources: (https://mpd.bioinf.uni-sb.de/mirna.html?mirna=hsa-miR-1976&organism=hsa), (https://mpd.bioinf.uni-sb.de/mirna.html?mirna=hsa-miR-1976&organism=mmu)
  2. It is very convenient to browse the data since it is organized first by species (human or mouse), then since the database is organized in a matrix, you can view the database and search through it by either the individual MiRNA and what pathways it is involved in or the pathways that contain the given kind of MiRNA.Source: (https://mpd.bioinf.uni-sb.de/pathways.html?organism=hsa)
  3. It is somewhat convenient to download the data. The raw data is first given in both .tar.gz format and .zip on a designated page. While .zip is the standard way to compress a file, a .tar.gz acts as a container for compressed files and unless you are using Linux or MacOS, you need a software to open it. Finally, each of the queries can be downloaded into a new spreadsheet in either .xlsx or .csv format, both of which are standard formats. Sources: (https://mpd.bioinf.uni-sb.de/download.html), (https://mpd.bioinf.uni-sb.de/pathway.html?database=KEGG&pathway=MicroRNAs%20in%20cancer&organism=hsa)
  4. I would say that the website is extremely well organized. It contains a very detailed tutorial in both a web page form and a .pdf download. The search options are very well-organized since they are separated by species, and the results can be either by pathway or by molecule. When I ran a query for the molecule "hsa-miR-1976" for example, two tables were returned that contained well organized-data that had their own search queries. Source: (https://mpd.bioinf.uni-sb.de/mirna.html?mirna=hsa-miR-1976&organism=hsa)
  5. There are no restrictions on access nor is there a license agreement to use the database. Source: (https://mpd.bioinf.uni-sb.de/about.html)

Building the Powerpoint

After we had both individually researched the answers to our questions, we met for multiple hours on the afternoon of October 2nd to go over the information we have found. After discussing our thoughts on the database, and deciding on how to best present the information, we started a presentation on Google Slides. We began working on the slides together during the remaining time we had together. We then broke up the remaining slides to complete separately in the evening. Through the Chat option on Google Slides and text messaging, we stayed in contact about our progress as we finished the project. Finally, we planned to meet a bit before class on October 3rd to run through the presentation once together.

Submission

Media:Quinn_Lanners_and_John_Lopez_Biological_Databases_evaluation_of_miRPathDB_Database.pptx

Acknowledgements

Quinn Lanners

  1. Quinn Lanners and John Lopez would like to thank each other for doing their part in the group project. By meeting once outside of class, and staying in contact throughout, we were able to work well together as a team.
  2. Google Slides for providing an effective platform from which to work together simultaneously on the presentation.

While I worked with the people noted above, this individual journal entry was completed by me and not copied from another source.
Qlanners (talk) 22:28, 2 October 2017 (PDT)

John Lopez

I worked with my partner Quinn Lanners in class Tuesday to pick out our gene and Thursday to organize how we would do the questions. I decided to solve the General Information and General Utility questions, while Quinn would solve the Scientific Utility and Summary questions. By the time we met up on Monday, October 2nd, we had all of the questions finished and began to work on the presentation that day. Quinn set up the presentation, title, and outline. We corresponded after our meeting to finish the powerpoint due to Google Drive. I worked on the slides that I would present in class, and Quinn worked on his. We met before class on Tuesday, October 3rd, in order to rehearse the presentation.

While I worked with the people noted above, this individual journal entry was completed by me and not copied from another source.

Johnllopez616 (talk) 23:02, 2 October 2017 (PDT)

References

Backes, C., Kehl, T., Stöckel, D., Fehlmann, T., Schneider, L., Meese, E., … Keller, A. (2017). miRPathDB: a new dictionary on microRNAs and target pathways. Oxford Academic. Retrieved on October 1, 2017 from https://academic.oup.com/nar/article/45/D1/D90/2290890/miRPathDB-a-new-dictionary-on-microRNAs-and-target
LMU BioDB 2017. (2017). Week 5. Retrieved October 1, 2017, from https://xmlpipedb.cs.lmu.edu/biodb/fall2017/index.php/Week_5
miRPathDB. (2016). Retrieved on October 1, 2017, from https://mpd.bioinf.uni-sb.de/documentation.html

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