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Videos
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Getting Started
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Catalog Panels
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What is a catalog panel?
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Inventoried vs Predesigned catalog panels
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Blood cancer-focused vs Solid tumor-focused panels
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Panel summary page
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Panel details page
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Downloaded Designer files
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Catalog Panel: Tumor Hotspot (THP)
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Catalog Panel: Myeloid
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Catalog Panel: Chronic Lymphocytic Leukemia (CLL)
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Catalog Panel: Acute Myeloid Leukemia (AML)
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What is a catalog panel?
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Custom Panels
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Custom Reference
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Targets and Amplicons
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Output Files
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Designer output files overview
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File: [panel-id].amplicons
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File: [panel-id]-amplicon.bed
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File: [panel-id].bed
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File: [panel-id]-coverage-summary.csv
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File: [panel-id]-design-summary.csv
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File: [panel-id]-insert.bed
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File: [panel-id].gatk
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File: [panel-id]-missed.bed
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File: [panel-id]-submitted.bed
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File: systemic-variants.blacklist
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Designer output files overview
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FAQs
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What does the error message "Invalid file format" mean?
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What should the reference FASTA file format be?
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What should the BED file format be?
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What does "Validated" mean for catalog panels?
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Why is my custom panel target invalid?
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Which mm10 chromosomes are supported?
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Do gene-based designs only include CDS regions?
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What are the typical processing times for Designer?
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What separator character should I use in a .csv file?
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Can I delete a custom panel order?
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How do I delete cookies and cache for Designer?
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Which files do I review to ensure my design is correct?
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What coordinate system does Designer use?
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How do I create a Mission Bio account?
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Why can’t I request a panel quote?
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Which catalog panels are available?
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Can the Designer panel file be used with Pipeline?
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Can I design my own targeted panel?
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Which reference genome does Designer use?
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Which hg19 chromosomes are supported?
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For chromosome X or Y, should X and Y be capitalized?
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How many amplicons can custom panels have?
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Where are the primer sequences for catalog panels?
-
Which sequencing platforms are supported?
-
How close can amplicons be?
-
Why are targets listed more than once in the output files?
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Why does coverage change when adding a transcript ID?
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Can I check if a variant is covered by an existing panel?
-
Which variants can be detected?
-
Do you support anything other than a human genome?
-
What does the error message "Invalid file format" mean?
-
Release Notes
-
Videos
-
Getting Started
-
Catalog Panels
-
What is a catalog panel?
-
Inventoried vs Predesigned catalog panels
-
Blood cancer-focused vs Solid tumor-focused panels
-
Panel summary page
-
Panel details page
-
Downloaded Designer files
-
Catalog Panel: Tumor Hotspot (THP)
-
Catalog Panel: Myeloid
-
Catalog Panel: Chronic Lymphocytic Leukemia (CLL)
-
Catalog Panel: Acute Myeloid Leukemia (AML)
-
What is a catalog panel?
-
Custom Panels
-
Custom Reference
-
Targets and Amplicons
-
Output Files
-
Designer output files overview
-
File: [panel-id].amplicons
-
File: [panel-id]-amplicon.bed
-
File: [panel-id].bed
-
File: [panel-id]-coverage-summary.csv
-
File: [panel-id]-design-summary.csv
-
File: [panel-id]-insert.bed
-
File: [panel-id].gatk
-
File: [panel-id]-missed.bed
-
File: [panel-id]-submitted.bed
-
File: systemic-variants.blacklist
-
Designer output files overview
-
FAQs
-
What does the error message "Invalid file format" mean?
-
What should the reference FASTA file format be?
-
What should the BED file format be?
-
What does "Validated" mean for catalog panels?
-
Why is my custom panel target invalid?
-
Which mm10 chromosomes are supported?
-
Do gene-based designs only include CDS regions?
-
What are the typical processing times for Designer?
-
What separator character should I use in a .csv file?
-
Can I delete a custom panel order?
-
How do I delete cookies and cache for Designer?
-
Which files do I review to ensure my design is correct?
-
What coordinate system does Designer use?
-
How do I create a Mission Bio account?
-
Why can’t I request a panel quote?
-
Which catalog panels are available?
-
Can the Designer panel file be used with Pipeline?
-
Can I design my own targeted panel?
-
Which reference genome does Designer use?
-
Which hg19 chromosomes are supported?
-
For chromosome X or Y, should X and Y be capitalized?
-
How many amplicons can custom panels have?
-
Where are the primer sequences for catalog panels?
-
Which sequencing platforms are supported?
-
How close can amplicons be?
-
Why are targets listed more than once in the output files?
-
Why does coverage change when adding a transcript ID?
-
Can I check if a variant is covered by an existing panel?
-
Which variants can be detected?
-
Do you support anything other than a human genome?
-
What does the error message "Invalid file format" mean?
-
Release Notes