From: Jim Procter
Date: Tue, 21 Apr 2020 16:39:33 +0000 (+0100)
Subject: JAL-3407 add and document ComputePeptideVariants.groovy
X-Git-Tag: Release_2_11_1_0~4^2
X-Git-Url: http://source.jalview.org/gitweb/?a=commitdiff_plain;h=cfcd397b19f70fb39d6d21437db8eb6ffcac3914;p=jalview.git
JAL-3407 add and document ComputePeptideVariants.groovy
---
diff --git a/examples/groovy/ComputePeptideVariants.groovy b/examples/groovy/ComputePeptideVariants.groovy
new file mode 100644
index 0000000..6caa69c
--- /dev/null
+++ b/examples/groovy/ComputePeptideVariants.groovy
@@ -0,0 +1,32 @@
+import jalview.datamodel.SequenceFeature
+import jalview.gui.Desktop
+def af = jalview.bin.Jalview.currentAlignFrame
+def av = af.viewport
+def fr = Desktop.getAlignFrameFor(av.codingComplement).getFeatureRenderer()
+def counts = 0
+def countm = 0
+for (seq in av.alignment.sequences)
+{
+ ds = seq.datasetSequence
+ for (res = ds.start ; res <= ds.end; res++)
+ {
+ mf = fr.findComplementFeaturesAtResidue(seq, res)
+ if (mf != null)
+ {
+ for (feature in mf.features)
+ {
+ variant = mf.findProteinVariants(feature)
+ if (!"".equals(variant))
+ {
+ type = variant.contains("=") ? "synonymous_variant" : "missense_variant"
+ if (type.equals("synonymous_variant")) counts++ else countm++;
+ sf = new SequenceFeature(type, variant, res, res, null)
+ seq.addSequenceFeature(sf)
+ }
+ }
+ }
+ }
+}
+af.getFeatureRenderer().featuresAdded()
+af.alignPanel.paintAlignment(true, true)
+println "Added " + countm + " missense and " + counts + " synonymous variants"
\ No newline at end of file
diff --git a/help/help/html/features/importvcf.html b/help/help/html/features/importvcf.html
index 511ff2e..7b699eb 100755
--- a/help/help/html/features/importvcf.html
+++ b/help/help/html/features/importvcf.html
@@ -72,6 +72,24 @@
for more information.
+ Working with variants without CSQ fields
+
+
+ Jalview 2.11.1's new virtual
+ features mean that peptide sequences are no longer annotated
+ directly with protein missense variants. This makes it harder to
+ filter variants when they do not already include the CSQ field. You
+ can rescue the pre-2.11.1 functionality by:
+
+
+ - Download the script at
+ https://www.jalview.org/examples/groovy/ComputePeptideVariants.groovy
+ - Executing the script via the Groovy
+ Console on a linked CDS/Protein view to create missense and
+ synonymous peptide variant features.
+
+
+
Working with variants from organisms other than
H.sapiens.
diff --git a/help/help/html/releases.html b/help/help/html/releases.html
index d3f2420..60e3179 100755
--- a/help/help/html/releases.html
+++ b/help/help/html/releases.html
@@ -139,6 +139,11 @@ li:before {
to stdout containing the consensus sequence for each
alignment in a Jalview session
+
+ ComputePeptideVariants.groovy to translate
+ genomic sequence_variant annotation from CDS as
+ missense_variant or synonymous_variant on protein products.
+
diff --git a/help/help/html/whatsNew.html b/help/help/html/whatsNew.html
index 00f9466..0f0c7f1 100755
--- a/help/help/html/whatsNew.html
+++ b/help/help/html/whatsNew.html
@@ -43,7 +43,13 @@
Sequence
Features dialog. This allows more analyses of nucleotide and
peptide sequence features on alignments in a more flexible and
- memory efficient way than in earlier versions.
+ memory efficient way than in earlier versions.
+ Note: Virtual features work best when variants are
+ annotated with CSQ fields. Please see this
+ Groovy script workaround if you are working with VCF files
+ without CSQ fields.
+
Improved VCF data import Standard attributes for
filtering variants (e.g. position, QUAL field etc) are now
|