Tweet
Does anyone know if there is any free software that allows trimming of .ab1 files using a quality score average window and can output .ab1 files? I think Chromas can do this, but it is not free.
-
-
I think the chromatogram explorer can do what you are looking for (http://www.dnabaser.com/download/chromatogram-explorer/)
The lite version is freeware and has almost all features. -
Thanks I will check it out.Comment
-
Have you tried with the software ABI Seq Scanner? Is free, but you have to do the trim manually. At the end you can save the edited .ab1 file..Comment
-
Does anyone know if there is any free software that allows trimming of .ab1 files using a quality score average window and can output .ab1 files? I think Chromas can do this, but it is not free.???
______________
GuLComment
-
-
Sequencher
Have you tried with Sequencher? You can use a demo version and in the section sequence>trim>trim parameters you can set your "personal trimming values", so perhaps you can save and export sequence. Try!Comment
-
Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...04-04-2024, 04:25 PM -
Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...03-22-2024, 06:39 AM
Comment