I have a data set containing about 3000 genes with their numerical expression values and P-values.That means each gene has one expression value and one P-value.Now How can I draw a heat map?
I have a data set containing about 3000 genes with their numerical expression values and P-values.That means each gene has one expression value and one P-value.Now How can I draw a heat map?
R is very good to explore your data and draw plots. Here is how to plot a heatmap using the heatmap
function.
## Some dummy data: 100 genes x 10 samples
d <- matrix(rnorm(1000),100)
rownames(d) <- paste("gene",1:100,sep="")
colnames(d) <- LETTERS[1:10]
head(d)
A B C D E F
gene1 -1.0362235 0.82685836 -0.3053555 -1.25348438 -1.1167804 -0.21246920
gene2 -1.0280138 -0.10380856 -0.4725301 -0.02306777 -0.6119725 0.10499482
gene3 -1.2072158 -0.09147717 0.2429783 0.18397650 -0.5749762 -0.82854688
gene4 1.3769346 -0.34478739 -1.6498159 -0.04752349 -0.3759327 0.04173142
gene5 -0.8177475 -0.20440739 -1.4889405 0.50194321 0.9544585 1.23902602
gene6 0.5511526 0.62477829 -0.2677255 -0.74236524 -0.1572775 0.91825030
G H I J
gene1 -0.9427938 -1.4545177 -1.0756554 -0.08241979
gene2 -1.7248344 -2.2090110 -1.5504237 -0.19954993
gene3 0.2018804 1.7318818 -1.8288649 0.58678452
gene4 0.2948888 -0.2522309 -1.1669122 -0.60243273
gene5 1.0042703 0.5899186 -0.4196320 -0.66348636
gene6 2.3309169 -1.0491888 0.3506227 -0.71594841
And now, the heatmap
function get the figure
heatmap(d)
See ?heatmap
for details and customisation. To read you data into R, see ?read.table
, assuming it is in a csv format, or similar.
Hope this helps.
EDIT: The dendrograms have been added automatically. In brief, the heatmap represents the values in your data matrix (scaled and centred by default) and the hierarchical clustering is performed along columns and rows using the hclust
function (see ?hclust
) based on eucledian distance (see ?dist
).
To draw then manually
dd <- matrix(rnorm(100),5,2)
distMatrix <- dist(dd) ## genes/lines -- use dist(t(dd)) for samples/columns
distMatrix
1 2 3 4
2 1.139330
3 2.764294 2.995049
4 1.654401 2.484039 1.677883
5 1.254484 1.291086 1.714694 1.483167
dendro <- hclust(distMatrix)
plot(dendro)
Hello,
Suppose that I have already downloaded GSE63706 and normalized that and I have a normalized text file now. and I have also a list of probesets (a text file of my interest probesets) in this array. I want to have a heat map showing the expression pattern of my interest probesets in this array, for example in this array I have 4 varieties and different tissues (rind and flesh) and phases (0,10,20,30,40 and 50 days after harvesting). Heatmaps showing the expression pattern of my probesets in varieties, tissues and phases I mean
Here is a GUI called Microarray Software Suite (MeV). It has quite a simple tab-delimited upload format and lots of other functions, besides heatmaps.
Another is called GenePattern, but I have not really looked at this, just seen papers that have used it.
Another choice is HeatmapGenerator, which draws heatmaps based on R's heatmap libraries directly within a user-friendly GUI environment.
Are you a bioinformatician or a biomedical researcher?
If you are a Biomedical researcher I would recommend Gene-E from the Broad Institute to generate heatmaps, calculate differential gene expression and clusterings, and GenePattern (also from the Broad) to to perform more advanced analyses such as GSEA.
If you have Affymetrix .CEL files and an excel spreadsheet with clinical annotations you can use InSilico DB to go from you .CEL files to a list of differential expressed genes in Gene-E in ~20 mintutes (registration and upload included). Large datasets take longer to upload.
Try HeatmapGenerator to produce heatmaps directly in R without needing to know how to program in R.
This can be helpful: https://blog.bioturing.com/2018/05/08/how-to-build-a-hierarchical-clustering-heatmap-with-biovinci/
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How come you have only one expression value per gene? This sound as you would have measured the expression for one sample. What does this p-value mean, then?
You mean cluster THEN draw a heat map?
@Laurent It's probably the P value for a present/absent call (e.g. from Illumina's BeadArray software), but Fahmida would have to confirm that.
This kind of questions has already been addressed (and answered) a few times. You can find some insights here:
@David Quigley -- Yes, that's what I thought too, but then the heatmap does not make too much sense.
Yup, David is right, the P-value is for a present/absent call. Thanks to all. but one another question If I have such a data set which I have mentioned earlier,that means 3000 gene and each has single expression level and P-value for a present and absent call and this set up is for all the 39 experimental condition,then can I do any meaningful statistical operation to this data set?
Hi every one
There are miRNA sets containing cancer and healthy samples. I want to identify miRNA probes that differentially expressed in healthy subjects and cancer patients by applying t-test. Is there any one can help?
Tnx!