Version: 3.18

Custom Annotations

Overview

While the team tries to keep data sources up-to-date, you might want to start incorporate new annotations ahead of our update cycle. Another common use case involves protected health information (PHI). Custom annotations are a mechanism that enables both use cases.

Here are some examples of how our collaborators use custom annotations:

associating context from both a patient-level and a patient cohort level with the variant annotations
adding content that is licensed (e.g. HGMD) to the variant annotations

At the moment, we have two different custom annotation file formats. One provides additional annotations to variants (both small variants and SVs) while the other caters to gene annotations.

In both cases, the custom annotation file format is a tab-delimited file that is separated into two parts: the header & the data.

The header is where you can customize how you want the data to appear in the JSON file and provide context about the genome assembly and how Nirvana should match the variants.

At Illumina, there are usually many components downstream of Nirvana that have to parse our annotations. If a customer provides a custom annotation, those downstream tools need to understand more about the data such as:

data type (e.g. number, boolean, or a string)
data category (e.g. is this an allele count, allele number, allele frequency, etc.)
associated population (i.e. if this is an allele frequency)

For each custom annotation, Nirvana uses this context to create a JSON schema that can be sent to downstream tools. If a tool knows that this is an allele frequency, it can validate user input to ensure that it's in the range of [0, 1].

Variant File Format

File Format

Nirvana expects plain text (or gzipped text) files. Using tools like Excel can add extra characters that can break parsing. We highly recommend creating and modifying these files with plain text editor like Notepad, Notepad++ or Atom.

Basic Allele Frequency Example

Create the Custom Annotation TSV

Imagine that you want to create a basic allele frequency custom annotation for small variants. If we visualized the tab-delimited file (TSV), it would look something like this:

Col 1	Col 2	Col 3	Col 4	Col 5
#title=MyDataSource
#assembly=GRCh38
#matchVariantsBy=allele
#CHROM	POS	REF	ALT	allAf
#categories	.	.	.	AlleleFrequency
#descriptions	.	.	.	ALL
#type	.	.	.	number
chr16	23603511	TGA	T	0.000006579
chr16	68801894	G	A	0.000006569
chr19	11107436	G	A	0.00003291

Here's the full TSV file.

Let's go over the header and discuss the contents:

title indicates the name of the JSON key
assembly indicates that this data is only valid for GRCh38.
matchVariantsBy indicates how annotations should be matched and reported. In this case annotations will be matched and reported by allele.
categories provides hints to downstream tools on how they might want to treat the data. In this case, we indicate that it's an allele frequency.
descriptions are used in special circumstances to provide more context. Even though column 5 is called allAf, it might not be clear to a downstream tool that this means a global allele frequency using all sub-populations. In this case, ALL indicates the intended population.
type indicates to downstream tools the data type. Since allele frequencies are numbers, we'll write number in this column.

Reference Base Checking

Nirvana validates all the reference bases in a custom annotation. If a variant or genomic region is specified that has the wrong reference base, an error will be produced.

Sorting

The variants within each chromosome must be sorted by genomic position.

Convert to Nirvana Format

First we need to convert the TSV file to Nirvana's native file format and let's put that file in a new directory called CA:

$ mkdir CA
$ dotnet bin/Release/netcoreapp2.1/SAUtils.dll customvar \
  -r Data/References/Homo_sapiens.GRCh38.Nirvana.dat -i MyDataSource.tsv -o CA
---------------------------------------------------------------------------
SAUtils                                             (c) 2020 Illumina, Inc.
Stromberg, Roy, Lajugie, Jiang, Li, and Kang                         3.12.0
---------------------------------------------------------------------------

Chromosome 16 completed in 00:00:00.1
Chromosome 19 completed in 00:00:00.0

Time: 00:00:00.2

Annotate with Nirvana

Let's annotate the following VCF (notice that it's one of the variants that we have in our custom annotation):

##fileformat=VCFv4.1
#CHROM  POS ID  REF ALT QUAL    FILTER  INFO
16  68801894    .   G   A   .   .   .

Here's the full VCF file.

Since Nirvana can handle multiple directories with external annotations, all we need to do is specify our new CA directory in addition to the normal Nirvana command-line.

$ dotnet bin/Release/netcoreapp2.1/Nirvana.dll -c Data/Cache/GRCh38/Both \
  -r Data/References/Homo_sapiens.GRCh38.Nirvana.dat \
  --sd Data/SupplementaryAnnotation/GRCh38 --sd CA -i TestCA.vcf -o TestCA
---------------------------------------------------------------------------
Nirvana                                             (c) 2020 Illumina, Inc.
Stromberg, Roy, Lajugie, Jiang, Li, and Kang                         3.12.0
---------------------------------------------------------------------------

Initialization                                         Time     Positions/s
---------------------------------------------------------------------------
Cache                                               00:00:01.8
SA Position Scan                                    00:00:00.0           19

Reference                                Preload    Annotation   Variants/s
---------------------------------------------------------------------------
chr16                                   00:00:00.2  00:00:01.3            1

Summary                                                Time         Percent
---------------------------------------------------------------------------
Initialization                                      00:00:01.9       25.5 %
Preload                                             00:00:00.2        3.3 %
Annotation                                          00:00:01.3       18.2 %

Time: 00:00:06.3

Investigate the Results

We would expect the following data to show up in our JSON output file:

      "variants": [
        {
          "vid": "16-68801894-G-A",
          "chromosome": "16",
          "begin": 68801894,
          "end": 68801894,
          "refAllele": "G",
          "altAllele": "A",
          "variantType": "SNV",
          "hgvsg": "NC_000016.10:g.68801894G>A",
          "phylopScore": 1,
          "MyDataSource": {
            "refAllele": "G",
            "altAllele": "A",
            "allAf": 7e-06
          },
          "clinvar": [

Here's the full JSON file.

Nirvana preserves up to 6 decimal places for allele frequency data.

Categories & Descriptions Example

Create the Custom Annotation TSV

Building on the previous example, we can add other types of annotations like predictions and general notes.

Col 1	Col 2	Col 3	Col 4	Col 5	Col 6	Col 7
#title=MyDataSource
#assembly=GRCh38
#matchVariantsBy=allele
#CHROM	POS	REF	ALT	allAf	pathogenicity	notes
#categories	.	.	.	AlleleFrequency	Prediction	.
#descriptions	.	.	.	ALL	.	.
#type	.	.	.	number	string	string
chr16	23603511	TGA	T	0.000006579	P	.
chr16	68801894	G	A	0.000006569	LP	Seen in case 123
chr19	11107436	G	A	0.00003291	.	.

Here's the full TSV file.

Placeholders

You can use a period to denote an empty value (much in the same way as periods are used in VCF files to signify missing values). While Nirvana also accepts empty columns in the TSV file, we use them in these examples to promote readability.

Let's go over what's new in this example:

Column 6 adds a field called pathogenicity which uses the Prediction category. When using this category, Nirvana will validate to make sure that the field contains either the abbreviations (B, LB, VUS, LP, and P) or the long-form equivalents (e.g. benign or pathogenic).
Column 7 adds a field called notes and it doesn't have a category or description. We're just going to use it to add some internal notes.

Annotate with Nirvana

Let's use a new VCF file. It includes all the same positions as our custom annotation file, but only the middle variant also matches the alternate allele (allele-specific match):

##fileformat=VCFv4.1
#CHROM  POS     ID      REF     ALT     QUAL    FILTER  INFO
16  23603511    .   TG  T   .   .   .
16  68801894    .   G   A   .   .   .
19  11107436    .   G   C   .   .   .

Here's the full VCF file.

Investigate the Results

Because we specified #matchVariantsBy=allele in our custom annotation file, only the middle variant will get an annotation:

      "variants": [
        {
          "vid": "16-68801894-G-A",
          "chromosome": "16",
          "begin": 68801894,
          "end": 68801894,
          "refAllele": "G",
          "altAllele": "A",
          "variantType": "SNV",
          "hgvsg": "NC_000016.10:g.68801894G>A",
          "phylopScore": 1,
          "MyDataSource": {
            "refAllele": "G",
            "altAllele": "A",
            "allAf": 7e-06,
            "pathogenicity": "LP",
            "notes": "Seen in case 123"
          },
          "clinvar": [

Here's the full JSON file.

Using Positional Matches

What would happen if we changed to #matchVariantsBy=position? Two things will happen. First, our positional variants will now match:

      "variants": [
        {
          "vid": "16-23603511-TG-T",
          "chromosome": "16",
          "begin": 23603512,
          "end": 23603512,
          "refAllele": "G",
          "altAllele": "-",
          "variantType": "deletion",
          "hgvsg": "NC_000016.10:g.23603512delG",
          "MyDataSource": [
            {
              "refAllele": "GA",
              "altAllele": "-",
              "allAf": 7e-06,
              "pathogenicity": "P"
            }
          ],
          "clinvar": [

In addition, you will now see an extra flag for our allele-specific variant:

      "variants": [
        {
          "vid": "16-68801894-G-A",
          "chromosome": "16",
          "begin": 68801894,
          "end": 68801894,
          "refAllele": "G",
          "altAllele": "A",
          "variantType": "SNV",
          "hgvsg": "NC_000016.10:g.68801894G>A",
          "phylopScore": 1,
          "MyDataSource": [
            {
              "refAllele": "G",
              "altAllele": "A",
              "allAf": 7e-06,
              "pathogenicity": "LP",
              "notes": "Seen in case 123",
              "isAlleleSpecific": true
            }
          ],
          "clinvar": [

Genomic Region Example

Create the Custom Annotation TSV

In the previous example, we added a note for the middle variant, but sometimes it's handy to annotate a genomic region. Consider the following example:

Col 1	Col 2	Col 3	Col 4	Col 5
#title=MyDataSource
#assembly=GRCh38
#matchVariantsBy=allele
#CHROM	POS	REF	END	notes
#categories	.	.	.	.
#descriptions	.	.	.	.
#type	.	.	.	string
chr16	20000000	T	70000000	Lots of false positives in this region

Here's the full TSV file.

Let's go over what's new in this example:

Column 5 now has a field called notes. In essence, it looks exactly like column 7 from our previous example.
The main difference is that now one of our custom annotation entries is actually a genomic region. Any variant that overlaps with that region will get a custom annotation.

In the previous example we learned about positional matching vs allele-specific matching. For genomic regions, #matchVariantsBy=allele and #matchVariantsBy=position produce the same result.

Annotate with Nirvana

Let's use the same VCF file as our previous example.

Investigate the Results

    {
      "chromosome": "16",
      "position": 23603511,
      "refAllele": "TG",
      "altAlleles": [
        "T"
      ],
      "cytogeneticBand": "16p12.2",
      "MyDataSource": [
        {
          "start": 20000000,
          "end": 70000000,
          "notes": "Lots of false positives in this region",
          "reciprocalOverlap": 0,
          "annotationOverlap": 0
        }
      ],
      "variants": [

Here's the full JSON file.

Reciprocal & Annotation Overlap

For all intervals, Nirvana internally calculates two overlaps: a variant overlap and an annotation overlap. Variant overlap is the percentage of the variant's length that is overlapped. Annotation overlap is the percentage of the annotation's length that is overlap.

Reciprocal overlap is the minimum of those two overlaps. Given that the annotation is 50 Mbp and the deletion is one 1 bp, both overlaps will be pretty close to 0.

We will also see this annotation for the other variant on chr16:

    {
      "chromosome": "16",
      "position": 68801894,
      "refAllele": "G",
      "altAlleles": [
        "A"
      ],
      "cytogeneticBand": "16q22.1",
      "MyDataSource": [
        {
          "start": 20000000,
          "end": 70000000,
          "notes": "Lots of false positives in this region",
          "reciprocalOverlap": 0,
          "annotationOverlap": 0
        }
      ],
      "variants": [

Genomic Regions for Structural Variants Example

Create the Custom Annotation TSV

Often we use genomic regions to represent other known CNVs and SVs in the genome. In this use case, we usually don't want to match these regions to other small variants. To force Nirvana to match regions only to other SVs, use the #matchVariantsBy=sv option in the header. Here is an example:

Col 1	Col 2	Col 3	Col 4	Col 5
#title=MyDataSource
#assembly=GRCh38
#matchVariantsBy=sv
#CHROM	POS	REF	END	notes
#categories	.	.	.	.
#descriptions	.	.	.	.
#type	.	.	.	string
chr16	20000000	T	70000000	Lots of false positives in this region

Here's the full TSV file.

Let's go over what's new in this example:

The main difference is the header field #matchVariantsBy=sv which indicates that only structural variants that overlap these genomic regions will receive annotations.

Annotate with Nirvana

Let's use a new VCF file. It contains the first variant from the previous file and a structural variant deletion- both of which overlap the given genomic region.

##fileformat=VCFv4.1
#CHROM  POS     ID      REF     ALT     QUAL    FILTER  INFO
16  23603511    .   TG  T   .   .   .
16  68801894    .   G   <DEL>   .   .   END=73683789;SVTYPE=DEL

Here's the full VCF file.

Investigate the Results

Note that this time, MyDataSource only showed up for the <DEL> and not the deletion 16-23603511-TG-T.

    {
      "chromosome": "16",
      "position": 23603511,
      "refAllele": "TG",
      "altAlleles": [
        "T"
      ],
      "cytogeneticBand": "16p12.2",
      "variants": [
     ...
     ...
    {
      "chromosome": "16",
      "position": 68801894,
      "svEnd": 73683789,
      "refAllele": "G",
      "altAlleles": [
        "<DEL>"
      ],
      "cytogeneticBand": "16q22.1-q22.3",
      "MyDataSource": [
        {
          "start": 20000000,
          "end": 70000000,
          "notes": "Lots of false positives in this region",
          "reciprocalOverlap": 0.02396,
          "annotationOverlap": 0.02396
        }
      ],
      "variants": [

Mixing Small Variants and Genomic Regions

Create the Custom Annotation TSV

Previously we looked at examples that either had small variants or genomic regions. Let's create a file that contains both:

Col 1	Col 2	Col 3	Col 4	Col 5	Col 6
#title=MyDataSource
#assembly=GRCh38
#matchVariantsBy=allele
#CHROM	POS	REF	ALT	END	notes
#categories	.	.	.	.	.
#descriptions	.	.	.	.	.
#type	.	.	.	.	string
chr16	23603511	TGA	T	.	.
chr16	68801894	G	A	.	.
chr19	11107436	G	A	.	.
chr21	10510818	C	.	10699435	Interval #1
chr21	10510818	C	<DEL>	10699435	Interval #2
chr22	12370388	T	T[chr22:12370729[	.	Known false-positive

Here's the full TSV file.

Let's go over what's new in this example:

Column 4 now has the REF field. Exception for the case listed below, this is only used by small variants or translocation breakends.
Column 5 now has the END field. This is only used by genomic regions.
There are two custom annotations on chr21 and the start and end coordinates look the same, so what's different? Interval #2 has a symbolic allele in the ALT column. When this is used in custom annotation, the start position is treated as the padding base (using VCF conventions). When Nirvana matches a variant to interval #2, it will ignore the padding base and consider the start position to be at position 10510819.

Annotate with Nirvana

Let's use a new VCF file to study how matching works for intervals #1 and #2:

##fileformat=VCFv4.1
#CHROM  POS ID  REF ALT QUAL    FILTER  INFO
21  10510818    .   C   <DUP>   .   .   END=10699435;SVTYPE=DUP
22  12370388    .   T   T[chr22:12370729[   .   .   SVTYPE=BND

Here's the full VCF file.

The first variant is similar to the custom annotation labelled "interval #2". Position 10510818 is the padding base, so it effectively starts at position 10510819.

Investigate the Results

  "positions": [
    {
      "chromosome": "21",
      "position": 10510818,
      "svEnd": 10699435,
      "refAllele": "C",
      "altAlleles": [
        "<DUP>"
      ],
      "cytogeneticBand": "21p11.2",
      "MyDataSource": [
        {
          "start": 10510818,
          "end": 10699435,
          "notes": "Interval #1",
          "reciprocalOverlap": 0.99999,
          "annotationOverlap": 0.99999
        },
        {
          "start": 10510819,
          "end": 10699435,
          "notes": "Interval #2",
          "reciprocalOverlap": 1,
          "annotationOverlap": 1
        }
      ],

Here's the full JSON file.

As expected, the variant and interval #2 have matching endpoints, therefore there is 100% overlap. Interval #1 technically starts 1 bp earlier, so its overlap 99.9%.

Further down the JSON file, we find the annotated translocation breakend:

      "variants": [
        {
          "vid": "22-12370388-T-T[chr22:12370729[",
          "chromosome": "22",
          "begin": 12370388,
          "end": 12370388,
          "isStructuralVariant": true,
          "refAllele": "T",
          "altAllele": "T[chr22:12370729[",
          "variantType": "translocation_breakend",
          "MyDataSource": {
            "refAllele": "T",
            "altAllele": "T[chr22:12370729[",
            "notes": "Known false-positive"
          }
        }

Gene File Format

Basic Gene Example

Create the Custom Annotation TSV

Previously we looked at examples that either had small variants or genomic regions, however, sometimes we would like to add custom gene annotations. The gene custom annotation file format looks slightly different:

Col 1	Col 2	Col 3	Col 4
#title=MyDataSource
#geneSymbol	geneId	phenotype	notes
#categories	.	.	.
#descriptions	.	.	.
#type	.	string	string
TP53	7157	Colorectal cancer, hereditary nonpolyposis, type 5	.
KRAS	ENSG00000133703	Mismatch repair cancer syndrome	Seen in cohort 123

Here's the full TSV file.

Let's go over what's in this example:

Column 2 has the geneId field. This can be either an Entrez Gene ID or an Ensembl ID.

Gene Symbols

Gene symbols are always in flux and are being updated on a daily basis at the NCBI and at HGNC. Due to this, Nirvana uses the geneId to match genes rather than the gene symbol. However, to make the custom annotation files easier to read, we've included the geneSymbol column as well.

Unknown Gene IDs

When Nirvana parses the gene custom annotation file, it will note any gene IDs that are currently not recognized in Nirvana. In such a case, Nirvana will display an error showing all the unrecognized gene IDs.

Annotate with Nirvana

Let's use a VCF file that contain variants in TP53 and KRAS:

##fileformat=VCFv4.1
#CHROM  POS ID  REF ALT QUAL    FILTER  INFO
12  25227255    .   A   T   .   .   .
17  7675074 .   C   A   .   .   .

Here's the full VCF file.

Investigate the Results

  "genes": [
    {
      "name": "KRAS",
      "clingenGeneValidity": [
        {
          "diseaseId": "MONDO_0009026",
          "disease": "Costello syndrome",
          "classification": "disputed",
          "classificationDate": "2018-07-24"
        }
      ],
      "clingenDosageSensitivityMap": {
        "haploinsufficiency": "no evidence to suggest that dosage sensitivity is associated with clinical phenotype",
        "triplosensitivity": "no evidence to suggest that dosage sensitivity is associated with clinical phenotype"
      },
      "gnomAD": {
        "pLi": 0.000788,
        "pRec": 0.789,
        "pNull": 0.21,
        "synZ": 0.336,
        "misZ": 2.32,
        "loeuf": 1.24
      },
      "MyDataSource": {
        "phenotype": "Mismatch repair cancer syndrome",
        "notes": "Seen in cohort 123"
      }
    },

This is the abbreviated output for KRAS. Here's the full JSON file if you want to see the complete KRAS entry.

Customizing the Header

Title

For the title, you can provide any string that hasn't already been used. The title should be unique.

caution

Make sure that the title does not conflict with other keys in the JSON file.

For small variants, you can't provide a title that conflicts with other keys in the variant object. Some examples of this would be vid, chromosome, transcripts, etc.. The title should also not conflict with other data source keys like clinvar or gnomad.

For structural variants, you can't provide a title that conflicts with other keys in the position object. Some examples of this would be chromosome, svLength, cytogeneticBand, etc. The title should also not conflict with other data source keys like clingen or dgv.

caution

Care should be taken not to annotate using multiple custom annotations that all use the same title.

Genome Assemblies

The following genome assemblies can be specified:

GRCh37
GRCh38

Matching Criteria

The matching criteria instructs how Nirvana should match a VCF variant to the custom annotation.

The following matching criteria can be specified:

allele - use this when you only want allele-specific matches. This is commonly the case when using allele frequency data sources like gnomAD
position - use this when you want positional matches. This is commonly used with disease phenotype data sources like ClinVar
sv - use this when you want to match to all other overlapping SVs. This use case arose when we were adding custom annotations for baseline copy number intervals along the genome.

Category	Description	Validation
AlleleCount	allele counts for a specific population	See the supported populations below
AlleleNumber	allele numbers for a specific population	See the supported populations below
AlleleFrequency	allele frequencies for a specific population	See the supported populations below
Prediction	ACMG-style pathogenicity classifications	• `benign` (B) • `likely benign` (LB) • `VUS` • `likely pathogenic` (LP) • `pathogenic` (P)
Filter	free text that signals downstream tools to add the column to the filter	Max 20 characters
Description	free-text description	Max 100 characters
Identifier	any ID	Max 50 characters
HomozygousCount	count of homozygous individuals for a specific population	See the supported populations below
Score	any score value	Any double-precision floating point number

Descriptions

Descriptions are used to add more context to the categories. For now, descriptions are mainly used to associate allele counts, numbers, and frequencies with their respective populations.

Populations

The following populations were specified in the HapMap project, 1000 Genomes Project, ExAC, and gnomAD.

Population Code	Super-population Code	Description
ACB	AFR	African Caribbeans in Barbados
AFR	AFR	African
ALL	ALL	All populations
AMR	AMR	Ad Mixed American
ASJ		Ashkenazi Jewish
ASW	AFR	Americans of African Ancestry in SW USA
BEB	SAS	Bengali from Bangladesh
CDX	EAS	Chinese Dai in Xishuangbanna, China
CEU	EUR	Utah Residents (CEPH) with Northern and Western European Ancestry
CHB	EAS	Han Chinese in Beijing, China
CHS	EAS	Southern Han Chinese
CLM	AMR	Colombians from Medellin, Colombia
EAS	EAS	East Asian
ESN	AFR	Esan in Nigeria
EUR	EUR	European
FIN	EUR	Finnish in Finland
GBR	EUR	British in England and Scotland
GIH	SAS	Gujarati Indian from Houston, Texas
GWD	AFR	Gambian in Western Divisions in the Gambia
IBS	EUR	Iberian population in Spain
ITU	SAS	Indian Telugu from the UK
JPT	EAS	Japanese in Tokyo, Japan
KHV	EAS	Kinh in Ho Chi Minh City, Vietnam
LWK	AFR	Luhya in Webuye, Kenya
MAG	AFR	Mandinka in the Gambia
MKK	AFR	Maasai in Kinyawa, Kenya
MSL	AFR	Mende in Sierra Leone
MXL	AMR	Mexican Ancestry from Los Angeles, USA
NFE	EUR	European (Non-Finnish)
OTH	OTH	Other
PEL	AMR	Peruvians from Lima, Peru
PJL	SAS	Punjabi from Lahore, Pakistan
PUR	AMR	Puerto Ricans from Puerto Rico
SAS	SAS	South Asian
STU	SAS	Sri Lankan Tamil from the UK
TSI	EUR	Toscani in Italia
YRI	AFR	Yoruba in Ibadan, Nigeria

Data Types

Each custom annotation can be one of the following data types:

bool - true or false
number - any integer or floating-point number
string - text

tip

For boolean variables, only keys with a true value will be output to the JSON object.

Using SAUtils

Nirvana includes a tool called SAUtils that converts various data sources into Nirvana's native binary format. The sub-commands customvar and customgene are used to specify a variant file or a gene file respectively.

Convert Variant File

dotnet bin/Release/netcoreapp2.1/SAUtils.dll customvar \
     -r Data/References/Homo_sapiens.GRCh37.Nirvana.dat \
     -i MyDataSource.tsv \
     -o SupplementaryAnnotation

the -r argument specifies the compressed reference path
the -i argument specifies the input TSV path
the -o argument specifies the output directory

Convert Gene File

dotnet bin/Release/netcoreapp2.1/SAUtils.dll customgene \
     --uga Nirvana_UGA.tsv \
     -i MyDataSource.tsv \
     -o SupplementaryAnnotation

the --uga argument specifies the Nirvana universal gene archive (UGA) path
the -i argument specifies the input TSV path
the -o argument specifies the output directory

Nirvana_UGA file

The Nirvana_UGA is not part of the official set of files retrieved using the Downloader utility. But it is available here.

Overview​

Variant File Format​

File Format

Basic Allele Frequency Example​

Create the Custom Annotation TSV​

Reference Base Checking

Sorting

Convert to Nirvana Format​

Annotate with Nirvana​

Investigate the Results​

Categories & Descriptions Example​

Create the Custom Annotation TSV​

Placeholders

Annotate with Nirvana​

Investigate the Results​

Using Positional Matches​

Genomic Region Example​

Create the Custom Annotation TSV​

Annotate with Nirvana​

Investigate the Results​

Reciprocal & Annotation Overlap

Genomic Regions for Structural Variants Example​

Create the Custom Annotation TSV​

Annotate with Nirvana​

Investigate the Results​

Mixing Small Variants and Genomic Regions​

Create the Custom Annotation TSV​

Annotate with Nirvana​

Investigate the Results​

Gene File Format​

Basic Gene Example​

Create the Custom Annotation TSV​

Gene Symbols

Unknown Gene IDs

Annotate with Nirvana​

Investigate the Results​

Customizing the Header​

Title​

caution

caution

Genome Assemblies​

Matching Criteria​

Categories​

Descriptions​

Populations​

Data Types​

tip

Using SAUtils​

Convert Variant File​

Convert Gene File​

Nirvana_UGA file

Overview

Variant File Format

Basic Allele Frequency Example

Create the Custom Annotation TSV

Convert to Nirvana Format

Annotate with Nirvana

Investigate the Results

Categories & Descriptions Example

Create the Custom Annotation TSV

Annotate with Nirvana

Investigate the Results

Using Positional Matches

Genomic Region Example

Create the Custom Annotation TSV

Annotate with Nirvana

Investigate the Results

Genomic Regions for Structural Variants Example

Create the Custom Annotation TSV

Annotate with Nirvana

Investigate the Results

Mixing Small Variants and Genomic Regions

Create the Custom Annotation TSV

Annotate with Nirvana

Investigate the Results

Gene File Format

Basic Gene Example

Create the Custom Annotation TSV

Annotate with Nirvana

Investigate the Results

Customizing the Header

Title

Genome Assemblies

Matching Criteria

Categories

Descriptions

Populations

Data Types

Using SAUtils

Convert Variant File

Convert Gene File