diplomsko delo
Abstract
V dobi hitrega napredka orodij za sekvenciranje nove generacije so bioinformatska orodja za obdelavo velike količine podatkov, ki ob tem nastane izrednega pomena. V zadnjih letih se vedno bolj uveljavlja metoda RNA-seq za raziskave v transkriptomiki. Pri tem nastanejo kratki odčitki, ki pa jih je potrebno v nadaljevanju sestaviti v najbolj verjetno obliko prepisanega gena. Pri sestavljanju prepisanih genov poznamo dva pristopa. Prvi je z genomom vodeno sestavljanje prepisanih genov, pri čemer odčitke poravnamo z referenčnim genomom. Drugi pristop pa je sestavljanje prepisanih genov de-novo, pri katerem odčitke sestavljamo brez referenčne matrice. Oba pristopa imata tako prednosti kot slabosti. Z genomom vodeno sestavljanje je primerno za sestavljanje prepisanih genov modelnih organizmov. Pri teh so genomi dobro anotirani in jih lahko uporabimo kot referenco za poravnavo odčitkov. Pristop de-novo pa je bolj primeren za organizme katerih genomov ne poznamo, še niso sekvencirani. Namen tega diplomskega dela je predstavitev obeh pristopov, pregled nekaterih orodij ter primerjava le teh.
Keywords
bioinformatika;bioinformacijska orodja;transkriptomika;sekvenciranje;genom;
Data
Language: |
Slovenian |
Year of publishing: |
2019 |
Typology: |
2.11 - Undergraduate Thesis |
Organization: |
UL BF - Biotechnical Faculty |
Publisher: |
[P. Jelovšek] |
UDC: |
601.4:575.116.4:577.212.3:575.112:004(043.2) |
COBISS: |
9366137
|
Views: |
687 |
Downloads: |
158 |
Average score: |
0 (0 votes) |
Metadata: |
|
Other data
Secondary language: |
English |
Secondary title: |
Comparison of bioinformatic tools for de-novo and genome guided assembly of transcribed genes |
Secondary abstract: |
In the age of fast development of tools for next-generation sequencing, the bioinformatics tools for processing of a large amount of data have an exceptional meaning. In the last few years, the RNA-seq method has established itself as a useful method in transcriptomics. Its output are short reads, which ha to be assembled in a possible transcripts. For transcript assembly two approaches are available. The first one is genome-guided assembly of transcripts. Using this approach the RNA-seq reads are aligned to the reference genome. The second approach is de-novo transcript assembly where we do not have the reference sequence, so the transcript is built from scratch. Both approaches have pros and cons. Genome guided assembly is appropriate for model organisms since their genomes are well annotated and used as a reference. De-novo approach is more appropriate for non-model organisms where genome sequence is not available. The purpose of this work is the presentation of both approaches, review of some commonly used tools and their comparison. |
Secondary keywords: |
bioinformatics;bioinformatic tools;transcriptomics;sequencing;genome; |
Type (COBISS): |
Bachelor thesis/paper |
Study programme: |
0 |
Embargo end date (OpenAIRE): |
1970-01-01 |
Thesis comment: |
Univ. v Ljubljani, Biotehniška fak., Študij biotehnologije |
Pages: |
VI, 17 str. |
ID: |
11217171 |