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esimonova.me
esimonova.me
Reputation:
30
Joined:
6.2 years ago
Last seen:
3.2 years ago
Location:
Czechia
Latest posts by user
0 votes
1 reply
721 views
resequensing of the whole sample or sequencing to X k reads and merging files
rna-seq sequencing-depth
updated by Ram Ram • written by esimonova.me • esimonova.me
0 votes
0 replies
0 views
Comment: Comment: Fastq Screen shows many unmapped reads
written by esimonova.me • esimonova.me
0 votes
2 replies
950 views
Fastq Screen shows many unmapped reads
fastq_screen
written by esimonova.me • esimonova.me
0 votes
0 replies
853 views
conumee - adding bed file instead of sample detailed regions
conumee r rtracklayer
written by esimonova.me • esimonova.me
0 votes
1 reply
1.1K views
Immune repertoire reconstruction from RNA-seq data
tcr-seq
updated by theHumanBorch • theHumanBorch • written by esimonova.me • esimonova.me
0 votes
0 replies
798 views
Genome reference with haplotypes
reference haplotypes
written by esimonova.me • esimonova.me
0 votes
1 reply
1.0K views
Deconvolution/quantification of immune cell types in Macaca Mulatta
rna-seq deconvolution
updated by İrem • İrem • written by esimonova.me • esimonova.me
0 votes
0 replies
0 views
Answer: Answer: Find Information about TCGA samples from GDC data portal
written by esimonova.me • esimonova.me
2 votes
4 replies
5.5K views
RNASEQ - Mapping to genome or Transcriptome
mapping rnaseq
updated by ponganta ponganta • written by esimonova.me • esimonova.me
0 votes
0 replies
0 views
Comment: Comment: Matplotlib comprehensive chromosome drawing
written by esimonova.me • esimonova.me
0 votes
1 reply
0 views
Comment: Comment: Strand specific library
written by esimonova.me • esimonova.me
0 votes
0 replies
0 views
Comment: Comment: Strand specific library
written by esimonova.me • esimonova.me
0 votes
6 replies
2.2K views
Strand specific library
htseq
updated by benformatics benformatics • written by esimonova.me • esimonova.me
0 votes
0 replies
1.2K views
mSINGs - pipeline
msi
written by esimonova.me • esimonova.me
0 votes
0 replies
835 views
Freebayes - too many variants produced on WES sample
freebayes
written by esimonova.me • esimonova.me
0 votes
0 replies
794 views
Simulated data or pseudoreplicatesreported in papers
pseudoreplicates snps indels
written by esimonova.me • esimonova.me
0 votes
0 replies
776 views
plink - generate VCF
plink
written by esimonova.me • esimonova.me
0 votes
1 reply
1.2K views
Precision of variant calling (INDELs)
indels hap.py
updated by desouzareis.r desouzareis.r • written by esimonova.me • esimonova.me
0 votes
0 replies
761 views
Validation of Bioinformatics pipeline with NA12763
hap.py
updated by Ram Ram • written by esimonova.me • esimonova.me
0 votes
0 replies
829 views
GATK VQSR filter
na12878 variantrecallibration
written by esimonova.me • esimonova.me
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