Hi all!
I am looking for a decent course in clinical exome analysis. I would prefer something in Europe and I am not excluding online courses...
26 results in 0.0030 seconds.
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A course in clinical exome analysis - any recommendations?
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How do you extract regions of interest when you have massive exome data?
Hi everyone,
I am new to bioinformatics and I have been having trouble with exome data. I've practised using standalone BLAST+ and I've... -
Amino Acid Sequence from Exome Data?
Hi Everyone,
I working on a project that requires an amino acid sequence of exome sequence data. My first approach was to use samtool's... -
GATK Based Variant calling STEPS
Hello,
I am working on putting together a workflow for calling variants using Haplotype called in GATK:
The process follow... -
Exome sequencing for homozygous recessive disease
I am naive in the field of genomics. Please guide me through these questions.
If I have exome sequencing data of a family with a homozygous... -
Reading a vcf - genotypes
Hi, I am trying to understand the genotype calls in my vcf, a trio.
Looking at one variant of interest, the calls are:
Dad Mum ... -
Determine ethnicity from exome sequence
I have data from 40 exomes and they are from de-identified post-mortem samples.
There are many SNPs that have a higher frequency in Asian... -
Mutect Analysis Criteria: Judgement Calls
Hello everybody, I am dealing with a dataset of cancer tumours sequenced on hiseq. I do not have a matched normal, and I have used Mutect to call somatic... -
RUbioSeq: a suite of parallelized pipelines for exome variation, CNVs and Bis-Seq
RUbioSeq has been developed to facilitate the primary and secondary analysis of resequencing projects by providing an integrated software suite of parallelized... -
Joint variant calling in trios
Hello,
I have exome sequencing data for a few sets of trios in which the offspring have phenotypically related but probably genetically... -
Illumina Truseq Exome 62Mb - variant metrics?
Hey Everyone,
I'm just curious what kind of variant metrics everyone obtains for the Truseq 62 Mb exome enrichment. I've only processed... -
Webinar: Assembling and Analyzing Illumina Data in Lasergene Genomics Suite
Join us for a webinar on Tuesday, March 12 at 12 PM EDT (GMT -4:00). DNASTAR's Matt Keyser will discuss our support for Illumina sequence assembly and... -
Exome data: how to filter by cases and controls?
Hi all,
I'm currently trying to figure out how to sort the exome data from several samples so that I would have a list with SNPs/indels... -
GeneTalk: a platform to find the second patient of its kind
Hi folks,
we started GeneTalk - a platform that is designed to find the second
patient of its kind. If you are analyzing a human... -
Exome Sequencing data
Hi,
This might be a naive question, but I am looking to download and analyze some exome sequencing data from the 1000 genome project website....
