Man page - hgvs2spdi(1)
Packages contains this manual
- join-into-groups-of(1)
- gbf2ref(1)
- quote-grouped-elements(1)
- disambiguate-nucleotides(1)
- gff-sort(1)
- pma2pme(1)
- pm-collect(1)
- pm-setup(1)
- systematic-mutations(1)
- sort-uniq-count-rank(1)
- archive-pids(1)
- efetch(1)
- pma2apa(1)
- gbf2fsa(1)
- intersect-uid-lists(1)
- skip-if-file-exists(1)
- archive-taxonomy(1)
- jsonl2xml(1)
- efetch.ncbi(1)
- difference-uid-lists(1)
- download-ncbi-data(1)
- snp2tbl(1)
- einfo(1)
- gbf2facds(1)
- tbl2prod(1)
- cit2pmid(1)
- run-ncbi-converter(1)
- args2slice(1)
- xy-plot(1)
- xml2tbl(1)
- archive-nihocc(1)
- fsa2xml(1)
- download-pubmed(1)
- just-top-hits(1)
- sort-uniq-count(1)
- sort-by-length(1)
- json2xml(1)
- filter-stop-words(1)
- archive-nmcds(1)
- print-missing-subranges(1)
- word-at-a-time(1)
- between-two-genes(1)
- esearch(1)
- xfilter(1)
- einfo.ncbi(1)
- efilter(1)
- gbf2info(1)
- pmc2bioc(1)
- download-ncbi-software(1)
- filter-columns(1)
- pm-refresh(1)
- edict(1)
- split-at-intron(1)
- amino-acid-composition(1)
- expand-current(1)
- gbf2xml(1)
- gff2xml(1)
- find-in-gene(1)
- archive-pmc(1)
- download-sequence(1)
- snp2hgvs(1)
- pmc2info(1)
- download-pmc(1)
- bsmp2info(1)
- pm-clean(1)
- esample(1)
- gene2range(1)
- print-columns(1)
- scn2xml(1)
- xfetch(1)
- archive-pubmed(1)
- ds2pme(1)
- tbl2xml(1)
- xml2fsa(1)
- xlink(1)
- download-flatfile(1)
- reorder-columns(1)
- blst2tkns(1)
- exclude-uid-lists(1)
- sort-table(1)
- fuse-segments(1)
- transmute(1)
- combine-uid-lists(1)
- pair-at-a-time(1)
- spdi2tbl(1)
- ecollect(1)
- accn-at-a-time(1)
- custom-index(1)
- gbf2tbl(1)
- align-columns(1)
- asn2ref(1)
- pm-prepare(1)
- elink(1)
- archive-nlmnlp(1)
- xtract(1)
- gm2segs(1)
- epost(1)
- hgvs2spdi(1)
- esummary(1)
- rchive(1)
- refseq-nm-cds(1)
- ini2xml(1)
- xinfo(1)
- xsearch(1)
- csv2xml(1)
- uniq-table(1)
- yaml2xml(1)
- ref2pmid(1)
- filter-record(1)
- fuse-ranges(1)
- nquire(1)
- filter-genbank(1)
Package: ncbi-entrez-direct
apt-get install ncbi-entrez-direct
apt-get install ncbi-entrez-direct
Manuals in package:
Documentations in package:
Manual
HGVS2SPDI
NAMESYNOPSIS
DESCRIPTION
SEE ALSO
NAME
hgvs2spdi - transform genomic variation data from HGVS to SPDI format
SYNOPSIS
hgvs2spdi
DESCRIPTION
hgvs2spdi reads records in the Human Genome Variation Society’s format from standard input and writes corresponding records in NCBI’s Sequence-Position-Deletion-Insertion format to standard output.
SEE ALSO
efetch (1), snp2hgvs (1), snp2tbl (1), spdi2tbl (1), xtract (1).