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Hengki Muradi
"[Salah satu tujuan dalam studi ekpresi gen (DNA/Protein) adalah menemukan subbagian
yang penting secara biologis dan kelompok-kelompok dari gen-gen. Pengelompokan gen tersebut dapat dilakukan dengan metode hirarki maupun metode partisi. Kedua metode pengelompokan dapat dikombinasikan, dimana
dilakukan fase partisi dan hirarki secara bergantian, metode ini dikenal dengan metode Hopach. Tahap partisi dapat dilakukan dengan metode PAM, SOM, atau K-Means. Proses partisi dilanjutkan dengan proses Ordered, baru kemudian dikoreksi dengan proses agglomorative, sehingga hasil pengelompokan menjadi lebih akurat. Dalam menentukan kelompok utama digunakan ukuran MSS (Median Split Silhouette). MSS mengukur homogenitas hasil pengelompokan,
dimana hasil pengelompokan yang dipilih adalah yang meminimumkan MSS. Pada pengelompokan 136 barisan DNA Virus Ebola dari GeneBank. Proses
awalnya dilakukan pensejajaran global, dan dilanjutkan dengan perhitungan jarak genetik dengan menggunakan koreksi Jukes-Cantor. Pada penelitian ini didapat jarak genetik maksimum adalah 0.6153407 sedangkan jarak genetik minimum adalah 0. Selanjutnya matriks jarak genetik dapat dijadikan dasar untuk mengelompokkan barisan-barisan tersebut dengan menggunakan metode Hopach. Pada hasil pengelompokan Hopach-PAM, diperoleh kelompok utama sebanyak 10 kelompok dengan nilai MSS sebesar 0,8873843. Kelompok-kelompok virus ebola dapat diidentifikasikan berdasarkan subspesies dan tahun pertama kali mewabah.
Proses pensejajaran global dan pengelompokan Hopach-PAM menggunakan bantuan program open source R.
......One goal in the study of gene expression (DNA/Protein) is finding biologically important subsets and clusters of genes. Clustering these genes can be achieved by hierarchical and partitioning methods. Both clustering methods can be combined, where partition and hierarchy phases can be executed alternately, this method is known as a Hopach method. The partitioning step can be done by the PAM, SOM, or K-Means clustering method. The partition process continued with the process of Ordered, then corrected with agglomorative process, so that the clustminering results become more accurate. The main clusters determine by using MSS
(Median Split Silhouette). MSS is used to measure homogeneity of the clustering result, in which the clustering is selected to minimize its MSS. The clustering procceses of 136 DNA sequences of Ebola virus, are started by performing a global alignment, and continued with the genetic distance calculations using
Jukes-Cantor correction. In this research we found the maximum genetic distance is 0.6153407, meanwhile the minimum genetic distance is 0. Furthermore, the genetic distance matrix can be used as a basis for clustering sequences in Hopach-PAM clustering method. Based on, the clustering results, we obtained 10 major clusters with MSS value of 0.8873843. Ebola virus clusters can be identified by subspecies and the first occoring year of their outbreak. We implemented the global alignment process and Hopach-PAM clustering algorithm using the open source program R.;One goal in the study of gene expression (DNA/Protein) is finding biologically important subsets and clusters of genes. Clustering these genes can be achieved by hierarchical and partitioning methods. Both clustering methods can be combined, where partition and hierarchy phases can be executed alternately, this method is known as a Hopach method. The partitioning step can be done by the PAM, SOM, K-Means clustering method. The partition process continued with the process
of Ordered, then corrected with agglomorative process, so that the clustmineringresults become more accurate. The main clusters determine by using MSS (Median Split Silhouette). MSS is used to measure homogeneity of the clustering result, in which the clustering is selected to minimize its MSS. The clustering procceses of 136 DNA sequences of Ebola virus, are started by performing a global alignment, and continued with the genetic distance calculations using Jukes-Cantor correction. In this research we found the maximum genetic distance is 0.6153407, meanwhile the minimum genetic distance is 0. Furthermore, the genetic distance matrix can be used as a basis for clustering sequences in Hopach-PAM clustering method. Based on, the clustering results, we obtained 10 major clusters with MSS value of 0.8873843. Ebola virus clusters can be identified by subspecies and the first occoring year of their outbreak. We implemented the global alignment process and Hopach-PAM clustering algorithm using the open
source program R., One goal in the study of gene expression (DNA/Protein) is finding biologically
important subsets and clusters of genes. Clustering these genes can be achieved by
hierarchical and partitioning methods. Both clustering methods can be combined,
where partition and hierarchy phases can be executed alternately, this method is
known as a Hopach method. The partitioning step can be done by the PAM, SOM,
or K-Means clustering method. The partition process continued with the process
of Ordered, then corrected with agglomorative process, so that the clustminering
results become more accurate. The main clusters determine by using MSS
(Median Split Silhouette). MSS is used to measure homogeneity of the clustering
result, in which the clustering is selected to minimize its MSS. The clustering
procceses of 136 DNA sequences of Ebola virus, are started by performing a
global alignment, and continued with the genetic distance calculations using
Jukes-Cantor correction. In this research we found the maximum genetic distance
is 0.6153407, meanwhile the minimum genetic distance is 0. Furthermore, the
genetic distance matrix can be used as a basis for clustering sequences in Hopach-
PAM clustering method. Based on, the clustering results, we obtained 10 major
clusters with MSS value of 0.8873843. Ebola virus clusters can be identified by
subspecies and the first occoring year of their outbreak. We implemented the
global alignment process and Hopach-PAM clustering algorithm using the open
source program R.]"
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2015
T43650
UI - Tesis Membership  Universitas Indonesia Library
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Andrei Bernadette
"Virus Ebola (EBOV) adalah salah satu virus paling mematikan di dunia yang memiliki virus wabah pada tahun 2014 di Afrika Barat. Ada lima jenis virus Ebola, Zaire (ZEBOV), Sudan (SEBOV), Pantai Gading (CEBOV), dan Bundibugyo (BEBOV). Virus ini sudah terbunuh sekitar 11.310 hidup dari 28.616 kasus, dan sampai sekarang tidak ada antivirus untuk EBOV. Salah satunya protein potensial yang bisa dihambat adalah Nucleoprotein (NP). EBOV NP ini memiliki fungsi sebagai replikasi virus dan perancah untuk protein virus tambahan. Dengan menghambat virus ini, itu dapat memotong replikasi RNA dan mengakhiri siklus hidup virus EBOV. Dari sebelumnya penelitian, Fu et al, menyatakan bahwa EBOV NP dapat disisipkan dengan asam 18β-glycyrrhetinic dan licochalcone A. Dalam penelitian ini, kami menggunakan modifikasi asam 18β-glycyrrhetinic dan licochalcone A menggunakan metode farmakofor untuk menghambat EBOV NP dan membandingkan yang terbaik ADMET mencetak skor untuk mendapatkan ligan baru sebagai penghambat nukleoprotein. Penelitian ini menggunakan MOE (Lingkungan Operasi Molekuler) 2014.09 dan DataWarrior v4.7.3. Ini dimodifikasi ligan ingin memiliki hasil yang lebih baik daripada ligan standar. Dalam penelitian ini, dimodifikasi senyawa 541 dari asam 18β-glycyrrhetinic dan senyawa termodifikasi 207 dari licochalcone A dipilih sebagai antivirus EBOV.

The Ebola Virus (EBOV) is one of the deadliest viruses in the world that had an outbreak virus in 2014 in West Africa. There are five types of Ebola viruses, Zaire (ZEBOV), Sudan (SEBOV), Ivory Coast (CEBOV), and Bundibugyo (BEBOV). This virus has been killed around 11,310 lives out of 28,616 cases, and until now there is no antivirus for EBOV. One of the potential proteins that can be inhibited is Nucleoprotein (NP). This EBOV NP has a function as a viral replication and scaffold for additional viral proteins. By inhibiting this virus, that can cut RNA replication and end the life cycle of the EBOV virus. From previous studies, Fu et al. Stated that EBOV NP can be inserted with 18β-glycyrrhetinic acid and
licochalcone A. In this study, we used a modification of 18β-glycyrrhetinic acid and licochalcone A used a pharmacophore method to inhibit EBOV NP and compared the best ADMET score to get a new ligand as a nucleoprotein inhibitor. This research uses MOE (Molecular Operating Environment) 2014.09 and DataWarrior v4.7.3. This modified ligand wants to have better results than standard ligands. In this study, it was modified compound 541 from 18β-glycyrrhetinic acid and 207 modified compound from licochalcone A selected as an EBOV antivirus.
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Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2019
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UI - Skripsi Membership  Universitas Indonesia Library