I have a multi-sample vcf file and I want to get a table of IDs on the left column with the variants in which they have an alternate allele in. It should look l
use-case
ansible-galaxy
spark-window-function
react-native-picker-select
tsne
hortonworks-sandbox
jitcode-jitcdde-jitcsde
pyscript
aubio
unfold
intersection
mathgl
redmine-api
appfuse
apple-watch-complication
vertx-verticle
objective-c
stylus-pen
parse-tree
mkmf
consul-health-check
response.contenttype
serial-port
react-native-device-info
pysmt
plotly-dash
angular-resolver
luarocks
apache-drill
desktop