Hacktoberfest 2026: die Issues, die Maintainer für den Oktober markiert haben – offen und einsteigerfreundlich. Hacktoberfest-Issues durchsuchen

Faithfully recapitulate metadata via a round-trip through `writeVcf` + `readVcf`.

Offen
#78 5 Kommentare 0 Reaktionen 0 zugewiesene Personen Auf GitHub ansehen

@jmg421 arbeitet bereits daran.

Seit 01.7.2026.

  • #101 von @jmg421 — offen

Bewertung

Schwierigkeit
4/5
Geschätzter Aufwand
3-5 Tage
Anfängerfreundlichkeit
55/100
Issue-Typ
Bug
Klarheit
Größtenteils klar
Aktivitätsstatus
Aktiv
Tech-Stack
r
Bereich
bioinformatics

Rechercherichtung

Beginne mit dem reproduzierbaren Beispiel structural.vcf und untersuche die writeVcf/readVcf-Behandlung von Metadaten, insbesondere contig-Headern, fileDate und Referenzinformationen. Verwende den roundtrip all.equal-Check als Regressionstest; abgeschlossen ist die Arbeit, wenn die gemeldeten Metadatenabweichungen behoben sind, ohne die beabsichtigte Provenienz zu verlieren.

Vom Indexierungsmodell aus dem Issue-Text verfasst.

Beschreibung

writeVcf performs some unnecessary work that interferes with a perfect roundtrip of a VCF to a file and back. At the very least, these discrepancies interfere with my unit tests that check for correct reproduction of a VCF object from a VCF file; they also have some practical consequences as they introduce differences in the MD5 checksums, which then prevents some deduplication mechanisms in backend storage systems. To illustrate:

fl <- system.file("extdata", "structural.vcf", package="VariantAnnotation")
out <- tempfile()
first <- readVcf(fl)
writeVcf(first, out)
roundtrip <- readVcf(out)

all.equal(roundtrip, first)
## [1] "Attributes: < Component “metadata”: Component “header”: Attributes: < Component “header”: Lengths: 9, 8 > >"
## [2] "Attributes: < Component “metadata”: Component “header”: Attributes: < Component “header”: Names: Lengths (9, 8) differ (string compare on first 8) > >"
## [3] "Attributes: < Component “metadata”: Component “header”: Attributes: < Component “header”: Attributes: < Component ## “listData”: Length mismatch: comparison on first 8 components > > >"
## [4] "Attributes: < Component “metadata”: Component “header”: Attributes: < Component “header”: Attributes: < Component “listData”: Component “fileDate”: Attributes: < Component “listData”: Component “Value”: 1 string mismatch > > > >"
## [5] "Attributes: < Component “metadata”: Component “header”: Attributes: < Component “reference”: Lengths (4, 0) differ (string compare on first 0) > >"

For mismatches 1-3: as documented in its manpage, writeVcf adds some ##contig headers based on the seqinfo() of the input object. However, in this case, all the sequence information is NA, so perhaps writeVcf might be smart enough to omit the ##contig headers altogether, rather than manufacturing some non-informative placeholders:

##contig=<ID=1>
##contig=<ID=2>
##contig=<ID=3>
##contig=<ID=4>

For mismatch 4: as documented, writeVcf replaces the fileDate with the current date. Perhaps you could consider an option to respect any existing date in the VCF object, which is useful for retaining provenance, e.g., if I'm using VariantAnnotation to make some changes to an existing VCF file but I want to keep the date of the original file's creation.

For mismatch 5: I'm not sure what happened here, but I'm guessing this has something to do with the extra contig lines.

Session information
R Under development (unstable) (2023-11-29 r85646)
Platform: aarch64-apple-darwin22.5.0
Running under: macOS Ventura 13.6.1

Matrix products: default
BLAS:   /Users/luna/Software/R/trunk/lib/libRblas.dylib
LAPACK: /Users/luna/Software/R/trunk/lib/libRlapack.dylib;  LAPACK version 3.11.0

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

time zone: America/Los_Angeles
tzcode source: internal

attached base packages:
[1] stats4    stats     graphics  grDevices utils     datasets  methods
[8] base

other attached packages:
 [1] VariantAnnotation_1.49.2    Rsamtools_2.19.2
 [3] Biostrings_2.71.1           XVector_0.43.0
 [5] SummarizedExperiment_1.33.1 Biobase_2.63.0
 [7] GenomicRanges_1.55.1        GenomeInfoDb_1.39.5
 [9] IRanges_2.37.0              S4Vectors_0.41.3
[11] MatrixGenerics_1.15.0       matrixStats_1.2.0
[13] BiocGenerics_0.49.1

loaded via a namespace (and not attached):
 [1] KEGGREST_1.43.0          rjson_0.2.21             lattice_0.22-5
 [4] vctrs_0.6.5              tools_4.4.0              bitops_1.0-7
 [7] generics_0.1.3           curl_5.2.0               parallel_4.4.0
[10] tibble_3.2.1             fansi_1.0.6              AnnotationDbi_1.65.2
[13] RSQLite_2.3.4            blob_1.2.4               pkgconfig_2.0.3
[16] Matrix_1.6-4             BSgenome_1.71.1          dbplyr_2.4.0
[19] lifecycle_1.0.4          GenomeInfoDbData_1.2.11  compiler_4.4.0
[22] stringr_1.5.1            progress_1.2.3           codetools_0.2-19
[25] yaml_2.3.8               RCurl_1.98-1.13          pillar_1.9.0
[28] crayon_1.5.2             BiocParallel_1.37.0      DelayedArray_0.29.0
[31] cachem_1.0.8             abind_1.4-5              tidyselect_1.2.0
[34] digest_0.6.33            stringi_1.8.3            restfulr_0.0.15
[37] dplyr_1.1.4              biomaRt_2.59.0           fastmap_1.1.1
[40] grid_4.4.0               cli_3.6.2                SparseArray_1.3.2
[43] magrittr_2.0.3           S4Arrays_1.3.1           GenomicFeatures_1.55.1
[46] XML_3.99-0.16            utf8_1.2.4               rappdirs_0.3.3
[49] filelock_1.0.3           prettyunits_1.2.0        bit64_4.0.5
[52] httr_1.4.7               bit_4.0.5                png_0.1-8
[55] hms_1.1.3                memoise_2.0.1            BiocIO_1.13.0
[58] BiocFileCache_2.11.1     rtracklayer_1.63.0       rlang_1.1.2
[61] glue_1.6.2               DBI_1.2.0                xml2_1.3.6
[64] R6_2.5.1                 GenomicAlignments_1.39.0 zlibbioc_1.49.0
Vorherrschende Sprache
R
Sterne
32
Forks
21
PR-Merge-Kennzahlen
Keine gemergten PRs in 30 T.

Entwicklungsumgebung

Dieses Projekt bietet weder Dev-Container noch Dockerfile noch Beitragsleitfaden – die Einrichtung liegt bei Ihnen. Beginnen Sie mit der README; die allgemeinen Schritte stehen in unserem Leitfaden für den ersten Beitrag.

Erste Schritte

  1. Lesen Sie das ganze Issue und danach den Beitragsleitfaden des Projekts.
  2. Schreiben Sie ins Issue, dass Sie es übernehmen — das erspart doppelte Arbeit.
  3. Forken Sie das Repository und arbeiten Sie in einem Branch.
  4. Öffnen Sie einen Pull Request, der die Issue-Nummer nennt.

Mehr aus Bioconductor/VariantAnnotation

Alle Issues in Bioconductor/VariantAnnotation

Ähnliche Issues

Weitere Issues zu R

Neue Issues direkt in Ihr Postfach

Eine kurze Übersicht über anfängerfreundliche GitHub-Issues.