Dump XML results from pubmed/Eutils
This program is now part of the main jvarkit
tool. See jvarkit for compiling.
Usage: java -jar dist/jvarkit.jar pubmeddump [options] Files
Usage: pubmeddump [options] Files
Options:
-e, --email
optional user email
-h, --help
print help and exit
--helpFormat
What kind of help. One of [usage,markdown,xml].
--ncbi-api-key
NCBI API Key see https://ncbiinsights.ncbi.nlm.nih.gov/2017/11/02/new-api-keys-for-the-e-utilities/
.If undefined, it will try to get in that order: 1) environment
variable ${NCBI_API_KEY} ; 2) the jvm property "ncbi.api.key" ; 3) A
java property file ${HOME}/.ncbi.properties and key api_key
-o, --output
Output file. Optional . Default: stdout
-r, --retmax
value for 'retmax' parameter for Eutils.
Default: 10000
-skip, --skip
[20180302] Optional set of elements names to be ignored in the output.
Spaces or comma separated. .eg: 'AuthorList PubmedData '
Default: <empty string>
--version
print version and exit
20140805
The project is licensed under the MIT license.
Should you cite pubmeddump ? https://github.com/mr-c/shouldacite/blob/master/should-I-cite-this-software.md
The current reference is:
http://dx.doi.org/10.6084/m9.figshare.1425030
Lindenbaum, Pierre (2015): JVarkit: java-based utilities for Bioinformatics. figshare. http://dx.doi.org/10.6084/m9.figshare.1425030
$ java -jar dist/pubmeddump.jar "Lindenbaum P" | grep ArticleTitle
<ArticleTitle>NGS library preparation may generate artifactual integration sites of AAV vectors.</ArticleTitle>
<ArticleTitle>Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.</ArticleTitle>
<ArticleTitle>[The Spanish Association of Surgeon's audited teaching programme for rectal cancer. Results after six years].</ArticleTitle>
<ArticleTitle>Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.</ArticleTitle>
<ArticleTitle>The 3rd DBCLS BioHackathon: improving life science data integration with Semantic Web technologies.</ArticleTitle>
<ArticleTitle>Mass spectrometry-based identification of native cardiac Nav1.5 channel alpha subunit phosphorylation sites.</ArticleTitle>
<ArticleTitle>BioStar: an online question & answer resource for the bioinformatics community.</ArticleTitle>
<ArticleTitle>Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME.</ArticleTitle>
<ArticleTitle>Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.</ArticleTitle>
<ArticleTitle>The Gene Wiki: community intelligence applied to human gene annotation.</ArticleTitle>
<ArticleTitle>Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.</ArticleTitle>
<ArticleTitle>Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.</ArticleTitle>
<ArticleTitle>Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.</ArticleTitle>
<ArticleTitle>RoXaN, a novel cellular protein containing TPR, LD, and zinc finger motifs, forms a ternary complex with eukaryotic initiation factor 4G and rotavirus NSP3.</ArticleTitle>
<ArticleTitle>CloneIt: finding cloning strategies, in-frame deletions and frameshifts.</ArticleTitle>
<ArticleTitle>In vivo and in vitro phosphorylation of rotavirus NSP5 correlates with its localization in viroplasms.</ArticleTitle>