bab72b3c808c25df14fb563dc33336ff79a1f629 kuhn Tue Apr 26 15:14:18 2022 -0700 moved canFam3 evaSnp track to top level for consistency with Lous pipeline. combined html page to include some extra info that was in the canFam3 page diff --git src/hg/makeDb/doc/canFam3.txt src/hg/makeDb/doc/canFam3.txt index 4382ae6..6bc195b 100644 --- src/hg/makeDb/doc/canFam3.txt +++ src/hg/makeDb/doc/canFam3.txt @@ -1308,30 +1308,33 @@ 3492428 BROAD_VGB_CANINE_PON_SNP_DISCOVERY 2458565 BROAD_DBSNP.2005.2.4.16.57 697053 TIGR_1.0 234166 BROAD_VGB_LYMPHOMA_SNP_DISCOVERY 4202 DOG_GEN_LAB_1032011 94 AMOUCD_MAL_20+TERV_1 ... cat evaSnps4.bed | awk '{print $10}' | sed -e "s/,/\n/g" | sort | uniq -c | sort -r # 52 # 52 different submitters. most from a few places, mostly the Broad ############################################################################## # canFam3 EVA SNPs (European Variation Archive) (DONE 2022-03-21 - b0b) +# NOTE: superceded by Lou's pipeline for consistency. +# doc'd for multiple assemblies at: evaSnp3.txt +# # adding VAI annotations # redoing the track after talking with Lou and standardinzing on data fields after VAI step # canFam3.1 = GCA_000002285.2 # get files (EVA Release 3) cd /hive/data/outside/dogSnps/release3 wget https://ftp.ebi.ac.uk/pub/databases/eva/rs_releases/release_3/by_species/canis_lupus_familiaris/GCA_000002285.2/GCA_000002285.2_current_ids.vcf.gz # what is .csi file???? # https://ftp.ebi.ac.uk/pub/databases/eva/rs_releases/release_3/by_species/canis_lupus_familiaris/GCA_000002285.2/GCA_000002285.2_current_ids.vcf.gz.csi # previous: # 5655125 evaRsIDs # same number in this release @@ -2035,24 +2038,16 @@ # complex_transcript_variant, # intron_variant, # non_coding_transcript_exon_variant, # upstream_gene_variant, # downstream_gene_variant, # intergenic_variant, # no_sequence_alteration, # add new filter lines to trackDb # filterValues.varClass (new name for same field -- orig EVA class # filterValues.ucscClass missense_variant,frameshift_variant,inframe_deletion,inframe_insertion,initiator_codon_variant,stop_gained,stop_lost,splice_acceptor_variant,splice_donor_variant,splice_region_variant,exon_loss_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,NMD_transcript_variant,synonymous_variant,stop_retained_variant,complex_transcript_variant,non_coding_transcript_exon_variant,intron_variant,upstream_gene_variant,downstream_gene_variant,intergenic_variant,no_sequence_alteration, # drop old filter lines (no longer using RS_VALIDATED field filterValues.valid No,Yes - - - - - - - - ##############################################################################