A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing...
247 results in 0.0052 seconds.
-
FINAL CALL - A Practical Introduction to NGS Data Analysis and Variant Calling (Munich, Germany | September 9–11, 2026)
Munich, Germany | September 9–11, 2026
A Practical Introduction to NGS Data Analysis and Variant Calling
Do you work with sequencing... -
10th Berlin Summer School in NGS Data Analysis (July 2026, in-person, Berlin) – registration open
Hi all,
We’re organizing our annual Berlin Summer School in NGS Data Analysis (June 15-19, 2026), and thought it may be of interest to this... -
9th Berlin Summer School in NGS Data Analysis 2025 (June 30 - July 4, 2025) -- SUMMER IN BERLIN --
9th Berlin Summer School in NGS Data Analysis 2025
When? June 30 - July 4, 2025
Where? Berlin, Germany
Link: www.ec... -
Final Call - Next-Generation Sequencing Data Analysis: A Practical Introduction (April 2-4 in Munich) - Two last seats
Advance your research. Understand NGS and analyze sequenced data yourself.
When? April 2-4, 2025
Where? Munich, Germany
... -
Whole Genome Sequencing Missing coverage in sequencing with Novaseq X Plus
Hello, unfortunately, our Whole Genome sequencing results given with 25B 2x151 cycle on Novaseq X Plus have started to show too many low coverage examples... -
Online Course - A Practical Introduction to NGS Data Analysis (February 10-12, 2025)
Online Course - A Practical Introduction to NGS Data Analysis
Quality Control, Read Mapping, Visualization and DNA Variant Analysis
... -
Online Workshop - A Practical Introduction to NGS Data Analysis (Dec 9-11, 2024)
Online Course - A Practical Introduction to NGS Data Analysis
Quality Control, Read Mapping, Visualization and DNA Variant Analysis
... -
Finding transcriptome matches for thousands of 21-mers
I have received a project and could use some advice.
My task is to find sequence matches in mRNA databases across 20+ taxa. I was presented... -
Using featureCounts on HISTA2 aligned data of the tomato genome
Hello there.
I am new with Bioinformatics and I am currently working on quantifying my genes in the RNA data that I received.
My workflow...Last edited by Antzel; 08-08-2024, 02:42 AM. -
Help needed to prepare consensus including overhangs
I am having trouble merging my pre-trimmed fastq files to merge with the inclusion of the overhangs/nonoverlapping reads at either end. have many files...
-
Online Course - A Practical Introduction to NGS Data Analysis (February 28 - March 1, 2024)
Online Course - A Practical Introduction to NGS Data Analysis
Quality Control, Read Mapping, Visualization and DNA Variant Analysis
When... -
NGS Data Analysis
Good day, All!
Please I need help regarding my DNA-sequence analysis. I have done alignment and variant calling on my DNA sequence, and have... -
Elevate Your NGS Skills: Join Our 2024 Online Course
Hello SeqAnswers Community,
Are you ready to take your Next-Generation Sequencing (NGS) skills to the next level? We're excited to announce... -
Elevate Your NGS Skills: Join Our 2024 Online Course
Hello SeqAnswers Community,
Are you ready to take your Next-Generation Sequencing (NGS) skills to the next level? We're excited to announce... -
accesing gene name RNAseq
hi
i am tryn to analysize RNAseq data by Kallisto to get the gene read count. after I get them, how can I reach to the gene I want? because it wont...
