More posts like this
-
Defining VNTR in BAM file by IGV
written by zizigoluHi I have `BAM` files for tumour and matched normal for my samples from WGS. By uploading `BAM` files in `IGV`, how I could know …
-
What is the different bewteen ucsc simple repeat and tandem repeat
written by octpus616 •Hi I noticed that UCSC has released various masks and annotations for the human reference genome, among which simple repeats and tandem repeats seem to …
-
Simple tandem repeat (STR) reference for hg38
written by Raman2 •Is there a comprehensive reference for all the STRs (Short tandem repeats) present in human genome? I looked into few different resources but couldn't get …
-
indication of N's sequences in reference genome
written by Nelislam4 •Hi, I just wanna know. What is the function of N's sequences in any reference genome? What is the indication of them in the reference …
-
Detect repeats problematic for PCR
written by mschmidI have a couple of target genomic regions from bacteria. Now I want to check if they are suitable to be templates for a PCR …
-
Looking for human reference genome with ancestral SNP alleles
written by ScottHi. I am looking for reference human genome fasta files (preferably hg38) where the SNP alleles contributing to the reference sequence are always the ancestral …
-
Tools for visualizing genome
written by arit.mhp •Hi BioStars, I need to visualize the genome sequence (mitochondrial and whole genome). Is there any tools to visualize the genome sequences. Basically I need …
-
copy number of genes
written by qwzhang0601I have a list of human genes, I want to check whether those genes have copy number variants in different species (e.g., human, mouse, or …
-
STR (short tandem repeats) ID from bam file?
written by RichardHi all, Are there any tools out there that are designed to extract the VNTR (variable number tandem repeats) for forensic testing from a bam …
-
What Genetic Marker To Use To Infer Pedigree From Sequencing Data?
written by michealsmith<p>Here's a unusual tricky question.</p> <p>Now I've got whole-exome sequencing data for 5 individuals from a family. However we don't know the pedigree. I'm just …
A comparison of the T2T with GRCh38 shows potentially some expanded regions of repeat sequence when you compare the T2T assembly with GRCh38 : https://www.ncbi.nlm.nih.gov/genome/cgv/browse/GCF_009914755.1/GCF_000001405.40/23025/9606#NC_060943.1:8832360-9318975/NC_000019.10:8729546-9185048/size=10000
Thank you very much
The link shows the MUC16 gene region, not the
Variable Number of Tandem Repeats (VNTRs). Do you know how to get the genomic coordinate of theVNTRin MUC16?Thank you
I was trying to show that depending on accuracy of assembly the information about VNTR will change. VNTR appear to be available from https://zenodo.org/record/8118376 (see the associated publication for details).
There appear to be other resources that you can explore: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234305/