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Transcript
UCSC Genome Browser
1
The Progress
Data from NCBI and TIGR
(www.ncbi.nlm.nih.gov and www.tigr.org )
Today - 85,759,586,764
Official “15 year”
Human Genome Project:
1990-2003
2
Database and Tool Explosion
The annual database
issue of Nucleic Acids
Research has grown
exponentially
1996: first annual
compilation of
databases and tools
lists 57 databases and
tools
2008: 1078 databases
and tools listed in
compilation
2000: 230 databases
and tools listed in
compilation
3
Genome Browsers
UCSC
Genome Browser
EBI
Ensembl
NCBI
Map Viewer
4
Organizing the Genome
Gene X
genes & predictions
variations and
repeats
Description
Transcript data
Structure
Gene Ontology
Pathway Data
Homologous
Genes
Expression Data
Etc….
cross-species
comparative data
and many more types of data from expression
and regulation to mRNA and ESTs…
5
UCSC Genome Browser: genome.ucsc.edu
UCSC Genome
Browser
7
Organization of genomic data…
Annotation Tracks
sequence Genome backbone: base position number
chromosome band
sts sites
gap locations
known genes
predicted genes
Links out to
more data
microarray/expression data
evolutionary conservation
SNPs
repeated regions
more…
8
gene details
Annotation Tracks
official
sequence
comparisons
SNPs
A sample of what we will find:
9
The Genome Browser Gateway
start page, basic search
text/ID
searches

Use this Gateway to search by:
◦
◦
◦
◦

Gene names, symbols
Chromosome number: chr7, or region: chr11:1038475-1075482
Keywords: kinase, receptor
IDs: NP, NM, OMIM, and more…
See lower part of page for help with format
10
The Genome Browser Gateway
start page choices, December 2006
1
2
3
4
5
6
Make your Gateway choices:
1. Select Clade
2. Select species: search 1 species at a time
3. Assembly: the official backbone DNA sequence
4. Position: location in the genome to examine
5. Image width: how many pixels in display window; 5000
max
6. Configure: make fonts bigger + other choices
11
The Genome Browser Gateway
sample search for Human TP53

Sample search: human, March 2006 assembly, tp53
select


Select from results list
ID search may go right to a viewer page, if unique
12
Overview of the whole
Genome Browser page
}
Genome viewer section
Groups of data
Mapping and Sequencing Tracks
Genes and Gene Prediction Tracks
mRNA and EST Tracks
Expression and Regulation
Comparative Genomics
Variation and Repeats
13
Sample Genome Viewer image,
TP53 region
base position
STS markers
Known genes
RefSeq genes
GenBank seqs
17 species compared
single species compared
SNPs
repeats
14
Visual Cues on the Genome
Browser
Tick marks; a single location (STS, SNP)
3' UTR
exon
<<<
exon
< exon < < < <ex 5' UTR
Intron, and direction of transcription <<< or >>>
Track colors may have meaning—for example, Known Gene track:
•If there is a corresponding PDB entry, = black
•If there is a corresponding NCBI Reviewed seq, = dark blue
•If there is a corresponding NCBI Provisional seq, = light blue
For some tracks, the height of a bar is increased likelihood
of an evolutionary relationship (conservation track)
15
Options for Changing Images:
Upper Section
Walk
left or
right
click to
zoom 3x
and re-center



Zoom
in
Specify
a
position
Zoom
out
fonts,
window,
more
Change your view or location with controls at
the top
Use “base” to get right down to the nucleotides
Configure: to change font, window size, more…
16
Annotation Track display options
enforce
changes
Links to info
and/or filters

Some data is ON or OFF by default
Change
track view

Menu links to info about the tracks: content, methods
You change the view with pulldown menus

After making changes, REFRESH to enforce the change

17
Annotation Track options, defined

Hide: removes a track from view

Dense: all items collapsed into a single line

Squish: each item = separate line, but 50% height + packed

Pack: each item separate, but efficiently stacked (full height)

Full: each item on separate line
18
Reset, Hide, Configure or Refresh to change
settings
enforce any changes
(hide, full, squish…)
reset, back
to defaults



start from
scratch
You control the views
Use pulldown menus
Configure options page
19
Click Any Viewer Object for Details
Click the item
New
web page
opens
Example: click your
mouse anywhere
on the TP53 line
Many details
and links
to more data
about TP53
20
informative
description
other resource links
Click annotation track item
for details pages
Not all genes have
links to sequences This much detail.
microarray data
Different
annotation tracks
carry different data.
mRNA secondary structure
protein domains/structure
homologs in other species
Gene Ontology™ descriptions
mRNA descriptions
pathways
21
Get DNA, with Extended Case/Color Options



Use the DNA link
at the top
Plain or Extended
options
Change colors,
fonts, etc.
22
Get Sequence from Details Pages
Click a track, go to Sequence section of details page
Click the line
Click the item
sequence section
on detail page
23
Accessing the BLAT tool
BLAT = BLAST-like Alignment Tool



Rapid searches by INDEXING the entire
genome
Works best with high similarity matches
See documentation and publication for details
◦ Kent, WJ. Genome Res. 2002. 12:656
24
BLAT tool overview:
Make
choices


Paste one
or more
sequences
DNA limit 25000 bases
Protein limit 10000 aa
25 total sequences
submit
Or
upload

25

go to alignment detail
go to browser/viewer
BLAT results, with links
sorting
Results with demo sequences, settings default; sort = Query, Score
◦ Score is a count of matches—higher number, better match


Click browser to go to Genome Browser image location (next slide)
Click details to see the alignment to genomic sequence (2nd slide)
26
BLAT results, browser link
click to flip frame
query




From browser click in BLAT results
A new line with your Sequence from BLAT Search
appears!
Watch out for reading frame! Click - - - > to flip frame
Base position = full and zoomed in enough to see
amino acids
27
BLAT results,
alignment details
Your query
Genomic match, color cues
Side-by-side alignment
yours
genomic
28
Proteome Browser

Access from homepage or
Known Gene pages


Exon diagram, amino
acids…
Many protein properties
(pI,
mw, composition, 3D…)
more
data
29
In-Silico PCR:
Find genomic sequence using primers





Select genome
Enter primers
Minimum 15
bases
Flip reverse
primer?
Submit
30