<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>DSpace Community: Internship Report I3L's Student</title>
  <link rel="alternate" href="http://http://repository.i3l.ac.id:80/handle/123456789/100" />
  <subtitle>Internship Report I3L's Student</subtitle>
  <id>http://http://repository.i3l.ac.id:80/handle/123456789/100</id>
  <updated>2026-04-21T15:20:23Z</updated>
  <dc:date>2026-04-21T15:20:23Z</dc:date>
  <entry>
    <title>Student Activity and Capstone Project in Machine Learning Cohort of Bangkit Academy 2024</title>
    <link rel="alternate" href="http://http://repository.i3l.ac.id:80/handle/123456789/1271" />
    <author>
      <name>Putta, Dhannyo</name>
    </author>
    <id>http://http://repository.i3l.ac.id:80/handle/123456789/1271</id>
    <updated>2025-05-08T04:19:59Z</updated>
    <published>2025-01-31T00:00:00Z</published>
    <summary type="text">Title: Student Activity and Capstone Project in Machine Learning Cohort of Bangkit Academy 2024
Authors: Putta, Dhannyo
Abstract: Bangkit Academy, part of the Study Independent MSIB program, ran from September 6 to December&#xD;
31, 2024, offering a comprehensive learning path in machine learning as part of this internship. Over&#xD;
the course of four months, the program featured a variety of activities, including online courses on&#xD;
Dicoding and Coursera, Instructor-Led Training (ILT), and the completion of a capstone group project.&#xD;
&#xD;
The machine learning courses covered intermediate to advanced topics, such as Python&#xD;
programming for operating systems, linear algebra for data science, supervised and unsupervised&#xD;
learning, TensorFlow for machine learning and deep learning, generative AI, and more. The ILT&#xD;
sessions were live online classes led by experts from leading companies, offering insights into the&#xD;
practical application of machine learning in the industry. The final capstone project encouraged&#xD;
collaboration between different learning paths to develop an app addressing real-world problems,&#xD;
integrating the knowledge and skills gained throughout the program.</summary>
    <dc:date>2025-01-31T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Molecular Dynamics Simulaon of the Fo Domain of Trypanosoma brucei FoF1-ATP Synthase to Uncover Water Channel Pathways</title>
    <link rel="alternate" href="http://http://repository.i3l.ac.id:80/handle/123456789/1270" />
    <author>
      <name>Shemuel, Josia</name>
    </author>
    <id>http://http://repository.i3l.ac.id:80/handle/123456789/1270</id>
    <updated>2025-05-08T04:14:02Z</updated>
    <published>2025-01-31T00:00:00Z</published>
    <summary type="text">Title: Molecular Dynamics Simulaon of the Fo Domain of Trypanosoma brucei FoF1-ATP Synthase to Uncover Water Channel Pathways
Authors: Shemuel, Josia
Abstract: Trypanosoma brucei is a unicellular parasite responsible for causing human African trypanosomiasis&#xD;
(HAT). The unique life cycle of the parasite, infecting tsetse flies and humans, is supported by its&#xD;
reversible FoF1-ATP synthase. The study aims to characterize the water channel pathways within the&#xD;
Fo domain of T. brucei FoF1-ATP synthase to elucidate its proton translocation mechanism. The Fo&#xD;
domain was inserted into POPC and DOPC membrane systems, with each membrane system being&#xD;
replicated three times. Equilibration and production simulation for each replicate was performed for&#xD;
20 ns and 100 ns, respectively. The lumenal and cytoplasmic half-channels were solvated in all&#xD;
replicates during the simulation, solvating the key-glutamate E102. A DOPC was shown to insulate&#xD;
the lumenal half-channel, replacing the role of the absent bH2. The lumenal half-channel was&#xD;
solvable through the rear entry, involving structurally determined key residues H75, H19, D202, and&#xD;
H155, as well as manually identified residues Y74, N150, and Y199. The cytoplasmic half-channel had&#xD;
a more open configuration, solvating key residues D223, R139, and R146, as well as manually&#xD;
identified residues E132, RQ219, S135, S142, and T143. The key-arginine was crucial in separating&#xD;
both half-channels; its rotamer is supported by coordinating water molecules with Q209.&#xD;
Phylogenetic analysis of subunit-a revealed that T. brucei is evolutionarily divergent from other&#xD;
species.</summary>
    <dc:date>2025-01-31T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Integrating tertiary structural representations for miRNA - drug interaction prediction</title>
    <link rel="alternate" href="http://http://repository.i3l.ac.id:80/handle/123456789/1268" />
    <author>
      <name>Margaretha, Febrina</name>
    </author>
    <id>http://http://repository.i3l.ac.id:80/handle/123456789/1268</id>
    <updated>2025-05-08T04:06:56Z</updated>
    <published>2025-01-31T00:00:00Z</published>
    <summary type="text">Title: Integrating tertiary structural representations for miRNA - drug interaction prediction
Authors: Margaretha, Febrina
Abstract: miRNAs are small non-coding RNAs that regulate gene expression and are dysregulated&#xD;
in many diseases. Its aberrant expression led to an interest in therapeutic intervention,&#xD;
where it can target drugs that are undruggable by proteins by acting as a gene regulator.&#xD;
Thus, exploring potential drugs from their aberrant miRNA information may facilitate&#xD;
novel treatments to tackle the current disease complexity. With the long process of&#xD;
wet-lab screening, it is imperative to provide a rapid miRNA and drug interaction&#xD;
screening to accelerate the drug discovery processes. This study proposes MDITransNet,&#xD;
a miRNA-drug interaction (MDI) neural network model that incorporates structural&#xD;
information of miRNA and molecular graphs of drugs that is trained under an adapted&#xD;
transformer block module of structure prediction. MDITransNet was able to retain a&#xD;
notable performance than conventional machine learning models with an area under the&#xD;
receiving operating curve (AUC) of 92% and 87% on the non-redundant test set, hairpin,&#xD;
and mature, respectively.</summary>
    <dc:date>2025-01-31T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Exploring Giant Virus (Nucleocytoviricota) Diversity Across Ecosystems from Viral Metagenomics Data</title>
    <link rel="alternate" href="http://http://repository.i3l.ac.id:80/handle/123456789/1267" />
    <author>
      <name>Heerlie, Devita Mayanda</name>
    </author>
    <id>http://http://repository.i3l.ac.id:80/handle/123456789/1267</id>
    <updated>2025-05-08T04:04:18Z</updated>
    <published>2025-01-31T00:00:00Z</published>
    <summary type="text">Title: Exploring Giant Virus (Nucleocytoviricota) Diversity Across Ecosystems from Viral Metagenomics Data
Authors: Heerlie, Devita Mayanda
Abstract: Giant viruses, belonging to the Nucleocytoviricota phylum, are abundant in marine&#xD;
environments but their role in these ecosystems remains largely unexplored. These large-genome&#xD;
viruses are crucial for shaping microbial communities in marine waters, influencing nutrient cycling&#xD;
and ecosystem dynamics. The diversity of giant viruses between two different environment,&#xD;
Southern East China Sea and Kenting National Park, was examined in this study using metagenomics&#xD;
in the through Metagenome Assembled Genome (MAG) analysis, going through the process of&#xD;
assembly, giant virus detection, mapping, sorting, binning, and dereplication. We identified 91 MAGs&#xD;
across four sampling sites. Phylogenetic analysis revealed that Imitervirales was the most abundant&#xD;
order in both environments. Sample 20104 from the Southern East China Sea was the most diverse,&#xD;
hosting two unique orders not found in other samples. Bray-Curtis Dissimilarity metrics indicated&#xD;
similar diversity between Southern East China Sea samples, while Kenting National Park samples&#xD;
were more distinct. Despite similar order-level composition, functional gene analysis showed&#xD;
significant differences between the sites, unique genes involves in signal transduction and immune&#xD;
system genes in the Southern East China Sea and unique fatty acid metabolism genes in Kenting&#xD;
National Park. This highlights giant viruses' distinct composition and function in these environments,&#xD;
emphasizing their role in influencing marine ecosystem health and stability.</summary>
    <dc:date>2025-01-31T00:00:00Z</dc:date>
  </entry>
</feed>

