last update: 23/02/2012
GenomeStudio is software by Illumina used to score SNPs based on the Illumina BeadExpress platform.
SNP calling is based on the ability to differentiate between three well-defined groups, two homozygotes and the heterozygotes. The less overlap there is between these groups, the better the SNP has been typed.
Populations should be scored separately. Different populations may have inversion differences, which will make mapping hard. If they have no common pedigrees, there is no advantage in scoring them together because no extra information becomes available. In contract, groups may be more obvious if scoring from a single populations is used.
Use all SNPs that you can, even if they are expected to be on the same genomic location. If they are, they can be removed at the mapping stage.
This is an iterative process, where each step affects previous steps and clarifies whether data look ok or not.
Remember to right click and select 'Recalculate statistics for all samples' in the samples table, after removing samples from the analysis.
Insert pedigree information
Pedigree information reveals scoring errors. Those errors may reflect errors in the pedigree file or the scoring, and can be used to clean up the data.
For the D. montana project, the names used in the pedigree file containing phenotypic information were bigger than the names on the eppendorfs containing the DNA, because the full name was too long to fit on eppendorfs. The pedigree name is a letter followed by a number and letters for each generation.
- For example K154DBA is a 'K' pedigree (Kuusamo-Finland, the other one would be 'V' for Vancouver-Canada), line 154, F3 generation (as DBA is three letters, one for each generation).
Once pedigree information is added, SNP typing incompatible with the pedigree is indicated on the SNP graph. Any samples run twice are also indicated:
X indicates offspring with PC or PPC[^PCexplanation] errors based on a given pedigree.
O indicates parents with PC or PPC errors.
Square indicates errors in reproducibility, i.e. when the same sample is genotyped twice and the two replicates fall into different groups.
[^PCexplanation]: Parent-Child or Parent-Parent-Child
Replicate samples give an idea of how well the typing works. Each sample must have an individual name, so the worse repeat is named to include 'repeat' in the end of its name.
Add replicate data
- Put all files from a BeadExpress run into a folder
File > Load Additional Samples > Load samples based on folder with intensities
For the D. montana project there are two pedigrees and three GenomeStudio files, one for each pedigree and one containing both. The additional run with replicate data contained individuals from both replicates.
For the individual pedigree files:
- Mark the files from the wrong pedigree for exclusion.
- Save a copy of the file as.
- Tick box to remove samples marked for exclusion.
- Right click on each sample in the Samples Table and edit the names
Define the replicate samples.
Analysis > Edit Replicates. Either import a text file where each row contains the names of the replicate samples, or define them from the 'Edit Replicates' popup window.
Remove worst replicate
Replicates could have been useful in defining groups to use for calling SNPs because they are expected to show the variance in calling the same sample.
Unfortunately the data were too messy in the D. montana project because the DNA extractions were not high quality. I decided to ignore the duplicate sample information and retained only the duplicate sample with most SNP calls:
- Sort by Sample ID in the Samples Table and look for the name of sample with 'repeat' next to it.
- Decide which run best by comparing the call frequency of these samples.
- Add the sample with the least SNP calls into the group 'worse repeat'. This is a group I made for the purpose.
- Right click, choose the 'worse repeat' samples, right click on one of them and 'exclude those samples from the analysis'.
- If the originally run sample was the worst, rename it by appending 'worse repeat' to its name, and rename the best repeat to just the sample name, so that it matches the pedigree name.
Add gender information
Gender can be useful in defining groups and identifying sex linked samples.
Create a .csv file with two columns,
Sample ID and
Create csv with sex information
The instructions assume there is an Excel file with the pedigree (ID, mother, father) and sex information, from which the correct columns need to be extracted.
To make the
sex.csvfile, copy the pedigree name along with the sex column. Copy both the pedigree individuals AND the parental generation, i.e. the generation with information on sex, but unknown parents. Paste to a new text file and convert to CSV[^convertCSVperl]. Add
Sample ID,Genderfor header.
Import in GenomeStudio
File > Import Phenotype Information from File...
[^convertCSVperl]: In the Terminal
perl -pe 's/\t/,/g' tabdelimitedFile.txt > sex.csv
Upon successful import, the Gender column of the samples should be populated. It may not be visible by default, but it is useful to be able to sort by this column. To make it visible using the interface from 'Column Chooser'.
Exclude all individuals with call rates < 0.65 and make clusters automatically
Manually re-cluster each locus
Zero SNPs if:
- They look ugly
- Have low normalised R (y axis on graph)
- Have too low polymorphisms to be useful
X-linked genes are expected to have more pedigree errors.
The general rule is to move and resize the clusters to minimise the number of pedigree errors. However some errors may be there as a consequence of inherent bad calling in the particular study (for example due to low DNA quality). So also try to define three separate clusters.
Holding Shift, click and drag the centre of a cluster to move it and click and drag on its edges to resize it. The number of pedigree errors is visible in the bottom of the Errors Table.
Remove individuals with low call rates relative to others
Once re-clustering is done, rank by call rate. Remove any individuals with relatively low call rates when compared to other individuals.
Identify sex linkage
To identify potential X linkage of a SNP, sort by Gender and then Het Excess. X-linked SNPs will have large and negative values for Het Excess. Visually, no male heterozygotes should exist on the graph showing the clusters.
If the DNA concentration of all samples was similar, males should have half the signal intensity than females, on X linked markers, because they contain a single copy of the SNP.
Remove mistyped males
Remove individual males that are heterozygous for X-linked loci, as judged by all other male data. If they are in HWE the loci may be autosomal after all.
Use duplicate samples to identify clusters
This approach did not work for the D. montana project. I kept the SNP run with the most calls amongst samples, see Remove worst replicate.
Minimise PPC errors
Exclude X-linked loci when estimating PPC errors.
Remove all individuals with high error rates, or check their pedigrees.
Remove loci with unusually high error rates.
Make a list with the names of X-linked markers
This is used later to modify genotyping information of the males for these markers, to help with genetic map construction.
Add the X-linked markers back to the data
Remove loci with high error rates
If any loci still have high error rates after excluding X-linked markers and pedigree errors, remove them.
Click on 'Report Wizard...'
Final Report > All Samples > 50th percentile GC score ? > Remove excluded samples from report > Remove zeroed SNPs from report > Matrix - do not Include GenCall score > Finish.
In the Terminal/Text editor
Make a SNP scoring file for R:
- Delete the first SNP report lines in a text editor.
- Transpose the file[^transposeLink]
perl transposeTabDelimited.pl inputFile.txt > SNPData.txt.
- Add 'ID' in the very beginning before the tab of the first line, to make it compatible for R import.
pedData.txt file. This should be tab-delimited, contain the same name of individuals as the
SNPData.txt and contain the headers:
ANIMAL_ID SIRE_ID DAM_ID
The following commands read the files and combine them based on the column names 'ANIMAL_ID' and 'ID', and export the merged information.
KData<-read.table("/Users/zabameos/Dropbox/GTD/Inbox/kdataManip/Ktransposed.txt", header=T) VData<-read.table("/Users/zabameos/Dropbox/GTD/Inbox/kdataManip/Vtransposed.txt", header=T) pedData<-read.table("/Users/zabameos/Dropbox/GTD/Inbox/kdataManip/pedData.txt", header=T) sexData<-read.table("/Users/zabameos/Dropbox/GTD/Inbox/kdataManip/aPedSex.txt", header=T) pedSexData=merge(pedData, sexData, by.x="ANIMAL_ID", by.y="Sample_ID", all=F ) mergedKData=merge(pedSexData, KData, by.x="ANIMAL_ID", by.y="ID", all=F ) mergedVData=merge(pedSexData, VData, by.x="ANIMAL_ID", by.y="ID", all=F ) write.table(mergedVData, file="VMerged.txt", quote=F, row.names=F, sep="\t") write.table(mergedKData, file="KMerged.txt", quote=F, row.names=F, sep="\t")
Back in the Terminal/Text editor
Generate a tab between each allele of a SNP and convert missing data to 0s:
perl -pe 's/\-\-/0\t0/g ; s/\t(\D)(\D)/\t$1\t$2/g' pedigreeMerged.txt > out.txt
In a text editor:
- Delete the first rows up to the sample names, the names of which have been scrambled.
- Copy the sample names from the
- For the first row (just copied) replace tabs with double tabs for the columns with marker names, and paste on the top of the file.
Check all is well by opening in Excel. The input crigen expects is of the form:
Change typing of males to make the X-chromosome mappable
Males should all be homozygotes for X markers, which is obvious for some markers in Genomestudio.
These males should be manually made heterozygote with another allele. However it must be one of the DNA letters, e.g.
T. Use anything other than what the males already are. The Pedigree file should also contain sex information.
Also take the opportunity to zero any heterozygote males.
Format the pedigree for crimap
Crimap does not accept letters on the pedigree names. Originally I used a perl script, however it did not result in unique names. I then manually changed the names by find and replace for all individuals in Excel to make sure the names are unique.
This also allowed to visualise how many of the parents are not scored, because I renamed sequentially based on the offspring row, so if some offspring were not there but were parents of other individuals, they would have kept their original names in the parent columns. I then sequentially renamed the parent columns.
It is useful to get a feel of the data by doing it manually, but it is much faster to do it in R.
Rename factors to numbers in R
First collect all columns from the pedigree files into a single column and sort alphabetically in Excel. Output as text as
pedigreeNames.txt, no header is needed. Also copy the first three columns of the excel file into a
correctVPed.txt file. Import both in R.
pedData<-read.table("/Users/zabameos/Desktop/temp/correctVPed.txt", header=T) pedigreeNames<-read.table("/Users/zabameos/Desktop/temp/pedigreeNames.txt", header=F)
The following code renames the individual names to numbers and applies the naming to the pedigree file.
oldNames <- unique(pedigreeNames$V1) newNames <- seq(1:length(oldNames)) nameData <- data.frame(oldNames, newNames) newID = merge(pedData, nameData, by.x="ANIMAL_ID", by.y="oldNames", all=F ) names(newID)[names(newID)=="newNames"] = "newID" newSireID = merge(newID, nameData, by.x="SIRE_ID", by.y="oldNames", all=F ) names(newSireID)[names(newSireID)=="newNames"] = "newSireID" newDamID = merge(newSireID, nameData, by.x="DAM_ID", by.y="oldNames", all=F ) names(newDamID)[names(newDamID)=="newNames"] = "newDamID" allPedigreeNames <- data.frame(newDamID) write.table(allPedigreeNames, file="allPedigreeNames.txt", quote=F, row.names=F, sep="\t")
The output file contains the original input pedigree and the new names.
- Replace the number that replaced
0in the original pedigree with
- Sort it by ID in Excel and make sure the Excel file is sorted by ID. Copy and paste the new names onto the old ones in Excel.
- Copy all data to a text file[^linuxBreak] and save with a
Congratulations! You have a file that can be used by Crigen.
Unexplained errors - Thoughts
It is not possible to unmark a sequence, so be careful of what markings you use.
Once some sequences are removed from the analysis, they need to be manually processed again. I encountered this when excluding the X linked markers for identifying real pedigree errors: they have to be clustered again manually.
Pedigree names were complicated to keep track of, and resulted in duplicate shortened names on the eppendorfs which were tricky to track down and had to be excluded. A better approach would have been to just name the individuals sequentially.
In some cases, mostly in the Vancouver pedigree (40 occasions compared to 8 in Oulanka) the SNPs of males would fail, while some female SNPs would work.
One possible explanation is that these are sex-linked markers and females have more targets that can amplify, and are therefore biased to work. In any case most of the samples did not work, so the SNPs were considered unscorable.
Action taken - SNPs considered unscorable, as some females would also fail. For example in the figure only 68 + 13 samples worked, so most samples failed.
Above-average pedigree errors
Both Vancouver and Oulanka had some pedigree errors even after carefully checking the pedigrees for duplicates, wrong names etc. The number of errors was similar for most SNPs and can be traced to its source. However some SNPs showed an uncharacteristically high number of pedigree errors. These may sometimes be removed by changing the group assignment manually.
There was usually no alternative group calling that reduced the number of errors. One possible source is multiple targets to the same SNP, for example if the SNPs are on transposable elements.
One possible explanation is that sequences with these SNPs are repetitive DNA, so there were multiple targets for them in the genome.
Action taken - Removed from the analysis.
Heterozygote-biased pedigree errors
For some samples most errors seemed to be on female heterozygotes (if there were male heterozygote errors the SNP might be sex-linked).
One possibility is that those samples are sex-linked, but were not called as such because there are data on only one homozygote. However in many cases they included females. The samples are particularly dodgy if one of the homozygotes is completely missing.
Action taken - Removed from the analysis.
X-linked marker deficit
In D. montana the X is the largest chromosome so about 25% of the markers were expected to be on it. Much fewer markers are X-linked. This may be because SNPs were called from both sexes, so there would be 75% coverage on the X compared to the autosomes, which may have biased against X-markers due to low reads achieved.
The golden rule of mapping is that 'No data is better than bad data'.
Pedigree errors show only some cases of bad SNP calls. Assuming that there are no pedigree errors[^pedigreeErrors], because the pedigree file has been checked specifically for them, the errors seen are due to wrong assignment of SNPs to groups. In general for the first attempts at mapping it is better to make the groups smaller and exclude individuals further away from the region showing pedigree errors. This ensures that the individuals with wrong genotypes are minimised.
Keep only pedigree individuals kept in scoring
Some individuals failed to score, even though there is pedigree information in them. It is a good idea to manually check which these individuals are to detect any mistakes.
In Excel, copy the original pedigree below the names of the scored samples. Make the original pedigree bold and sort by individual ID.
Cut and pasted any parents of rows that existed in the scored pedigree (they are one row below or above). This is a manual step but important to identify any leftover mistakes in the pedigree structure, for example the same individual ID having multiple parent pairs.
This needs to be done once. The final output is the
pedData.txt, which can be used to automatically add pedigree information to other files, such as SNP scoring from GenomeStudio or individual phenotypic information from other text files.
[^pedigreeErrors]: Real pedigree errors can be picked up during mapping.
[^transposeLink]: Use the perl script transposeTabDelimited.pl. It is possible to transpose in Excel too (select all)
copy > paste special > (tick) transpose
[^linuxBreak]: Don't save from Excel, because the
.gen file needs to have Linux line format line endings.
The original Crimap is out of date. It was first written when allozymes were the prevalent molecular markers. Consequently, it has some problems dealing with large pedigrees and large numbers of markers that article available for analysis today.
To deal with this we use the Crigen suite of programs, which prepare text files to make Crimap more capable and efficient with handling modern datasets which are larger and more complicated.
An improved version of Crimap was produced by Jill Maddox and Ian Evans (2.504) which is generally better than the old. However the Crigen suite of programs is not compatible with the improved Crimap.
Consequently, analysis starts with Crigen, then the old Crimap, then continues with Crigen (Autogroup) to produce chromosome-specific files, and then moves to the new Crimap which is better for the analysis.
Michael D Grosz and Monsanto have been providing the Crigen code to researchers to serve the community, and have kindly granted permission to distribute the Crigen programs through this site.
Jill Maddox and Ian Evans, who are still developing the improved Crimap, provide it for free through the animal genome website. Downloading requires to fill a short form with information on how it is used. It is important to provide as much information as possible, to help with making sure it works properly with current experimental designs, and to help with funding which is easier if a large user base can be demonstrated.
It is best to compile Crimap on the particular machine or OS used, to make sure it works with the available memory efficiently. For example it is possible fora pre-compiled version to crash when it runs out of memory, but a version compiled on the same machine to work fine. In practice, a pre-compiled version should work well enough, except if it crashes, in which case you should compile your own version which may not crash.
In practice I start the analysis with Crimap 2.4 and Crigen on Ubuntu Linux, running on a virtual machine on MacOSX because I could not compile the old programs in a modern machine. I then continue to the Crimap 2.5 which can be compiled on MacOSX (see Installation Instructions)
All commands have more options with which to run, however the following steps can be used as a backbone of the analysis. The full options are available from the three manuals that come with Crimap.
Prepare a .gen file
The general format of a .gen file is shown in the table.
ANIMAL_ID SIRE_ID DAM_ID Marker1 Marker2 Marker3 1 0 0 A C A T A A 2 0 0 A C A G A C 3 1 2 A C A G A C
Individuals must be named with numbers.
Sex-linked markers will be homozygotes for one sex (for example in males in Drosophila). Edit their genotyping so they are heterozygous, with one allele not present in females. For example a locus which is scored as either A or T and in males is either AA or TT should be changed in males to become AC or TC. Alternatively, the non existent allele can be set to
Full instructions on how to prepare a
.gen file from GenomeStudio are at the my GenomeStudio workflow.
Generate a Twopoint file for Autogroup
Separate the pedigree into families of about 50 individuals for 3 generations. These files are easier for Crimap to work with.
./crigen -g myData.gen -o 10 -size 50 -gen 3 ./crimap 10 prepare
choose no no no and then option 7 (twopoint) yes yes
Note, segmentation errors can be reported during the 'prepare' command. I found that they were resolved by choosing Linux encoding for line endings in the
.gen file. This is the default way text files are saved from BBEdit or Textmate.
## How to install perlprimer
Instructions edited from [here](http://perlprimer.sourceforge.net/download.html).
This worked on 30/09/2014 for two independent computers.
It is important to follow the steps in order. Makefiles made when one of the preceding steps was not performed will not work even after the step is performed. In that case, delete the folder and start by unzipping the downloaded file of the particular program.
### 1. Start with Perl >= 5.8.1.
My mac had 5.16.2
### 2. Install libwww-perl.
Run the following, as in the readme file
sudo make install
### 3. Install Xcode from the app store
Once downloaded, run it once so it installs stuff.
### 4. Install X11
Through [xquartz](http://xquartz.macosforge.org/landing/). Run the dmg file installer.
Restart the computer.
### 5. Install Perl/Tk from CPAN
[Download](http://search.cpan.org/~ni-s/Tk/) latest release
sudo make install
### 6. Install Spidey executable from NCBI
Add it to the command path (e.g. /usr/local/bin)
### 7. Download Perlprimer
[Perlprimer source (.zip archive)](http://perlprimer.sourceforge.net/download.html).
To run, go to the Perlprimer folder and run
It should open a GUI.