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Tekijä: | Eraslan, Gokcen |
Työn nimi: | A Dirichlet-Multinomial Mixture Model For Clustering Heterogeneous Epigenomics Data |
Julkaisutyyppi: | Diplomityö |
Julkaisuvuosi: | 2014 |
Sivut: | vi + 55 s. + liitt. 17 Kieli: eng |
Koulu/Laitos/Osasto: | Perustieteiden korkeakoulu |
Oppiaine: | Computational Systems Biology (IL3013) |
Valvoja: | Lähdesmäki, Harri ; Lagergren, Jens |
Ohjaaja: | Osmala, Maria |
Elektroninen julkaisu: | http://urn.fi/URN:NBN:fi:aalto-201410062747 |
OEVS: | Sähköinen arkistokappale on luettavissa Aalto Thesis Databasen kautta.
Ohje Digitaalisten opinnäytteiden lukeminen Aalto-yliopiston Harald Herlin -oppimiskeskuksen suljetussa verkossaOppimiskeskuksen suljetussa verkossa voi lukea sellaisia digitaalisia ja digitoituja opinnäytteitä, joille ei ole saatu julkaisulupaa avoimessa verkossa. Oppimiskeskuksen yhteystiedot ja aukioloajat: https://learningcentre.aalto.fi/fi/harald-herlin-oppimiskeskus/ Opinnäytteitä voi lukea Oppimiskeskuksen asiakaskoneilla, joita löytyy kaikista kerroksista.
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Sijainti: | P1 Ark Aalto 1730 | Arkisto |
Avainsanat: | chromatin enhancers promoters multi-view clustering histone modifications epigenomics generative models Dirichlet-multinomial mixture model |
Tiivistelmä (eng): | Epigenetic information sheds light on essential biological mechanisms including the regulation of gene expression. Among the major epigenetic mechanisms are histone tail modifications which can be utilized to identify cis-regulatory elements such as promoters and enhancers. Nucleosome positions and open chromatin regions are other key elements of the epigenomic landscape. Thanks to the advances in high-throughput sequencing technologies, comprehensive genome-wide analyses of epigenetic signatures are possible at present. Despite the growing number of epigenetic datasets, the tools to discover novel patterns and combinatorial presence of epigenetic elements are still needed. In this thesis, we introduce a model-based clustering approach that uncovers epigenetic patterns by integrating multiple data tracks in a multi-view fashion where different views correspond to different epigenetic signals extracted from the same genomic location. Moreover, to address the inaccuracy of the positions of anchor points, such as TF ChIP-seq peak summits or TSS, a profile shifting feature is implemented. Finally, owing to the hyperprior regularization, our approach can also account for the correlation between the number of reads mapped to consecutive base pair positions. We demonstrate that the genome-wide clustering of promoter and enhancer regions in human genome reveals distinct patterns in various histone modification and transcription factor ChIP-seq profiles. Furthermore, TFBS enrichment in different classes of enhancers and promoters that are identified by our method is investigated which shows that some transcription factors are significantly enriched in a subset of enhancer and promoter clusters. |
ED: | 2014-10-05 |
INSSI tietueen numero: 49807
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