Phylogeny: GISAID Track Settings
Phylogenetic Tree and Nucleotide Substitution Mutations in High-coverage Sequences in GISAID EpiCoV TM   (All Variation and Repeats tracks)

Display mode:       Reset to defaults

Sample sorting display

Enable Sample sorting display
Sample sorting order:
using the tree specified in file associated with track
using middle variant in viewing window as anchor.
Samples are clustered by similarity around a central variant. Samples are reordered for display using the clustering tree, which is drawn in the left label area.
To anchor the sorting to a particular variant, click on the variant in the genome browser, and then click on the 'Use this variant' button on the next page.
using the order in which samples appear in the underlying VCF file
Sample coloring scheme for tree:
Allele coloring scheme:
reference alleles invisible, alternate alleles in black
reference alleles invisible, alternate alleles in red for non-synonymous, green for synonymous, blue for UTR/noncoding, black otherwise
reference alleles in blue, alternate alleles in red
first base of allele (A = red, C = blue, G = green, T = magenta)
Sample sorting display height:
Minimum minor allele frequency (if INFO column includes AF or AC+AN):

VCF configuration help

List subtracks: only selected/visible    all  
 Min alt AF 1%  Nucleotide Substitution Mutations with Alternate Allele Frequency >= 1% in GISAID EpiCov TM Sequences    
 Min alt AF 0.1%  Nucleotide Substitution Mutations with Alternate Allele Frequency >= 0.1% in GISAID EpiCov TM Sequences    
 All (slow!)  All Nucleotide Substitution Mutations in GISAID EpiCov TM Sequences (slow at whole-genome scale)    
Source data version: 28-10-20


This track displays a phylogenetic tree inferred from SARS-CoV-2 genome sequences collected by GISAID, and mutations found in the sequences. By default, only very common mutations (alternate allele found in at least 1% of samples) are displayed, but other subtracks may be made visible in order to see more rare mutations. The phylogenetic tree is inferred by Rob Lanfear's sarscov2phylo pipeline. For display in the narrow space to the left of the main genome browser image, nodes in the tree are collapsed unless a mutation is associated with a node; i.e. the only branching points displayed are those at which mutations occurred.

Two options for coloring the tree, by Pangolin lineage (Rambaut et al.) or GISAID clade, are available. Both coloring schemes are adapted from Figure 1 of (Alm et al.) which presents a unified view of a simplified phylogenetic tree, Pangolin lineages, Nextstrain clades and GISAID clades.

colorlineage(s)Nextstrain cladeGISAID clade
      A 19B S
      B.n (n > 1) 19A L
      n/a (color not used when coloring by lineage; overlaps on tree with B.4 - B.7) n/a (overlaps on tree with 19A) O
      n/a (color not used when coloring by lineage; overlaps on tree with B.2) n/a (overlaps on tree with 19A) V
      B.1.5, B.1.6, B.1.8, other B.1.n that overlap GISAID clade G 20A (partial) G
      B.1.9, B.1.13, B.1.22, B.1.22, B.1.36, B.1.37 20A (partial) GH (partial)
      B.1.3, B.1.12, B.1.26, other B.1.n that overlap GISAID clade GH 20C GH (partial)
      B.1.1 20B GR

Display Conventions

In "dense" mode, a vertical line is drawn at each position where there is a mutation. In "pack" mode, the display shows a plot of all samples' mutations, with samples ordered using the phylogenetic tree in order to highlight patterns of linkage.

Each sample is placed in a horizontal row of pixels; when the number of samples exceeds the number of vertical pixels for the track, multiple samples fall in the same pixel row and pixels are averaged across samples.

Each mutation is a vertical bar at its position in the SARS-CoV-2 genome with white (invisible) representing the reference allele; the non-reference allele is shown in red if it changes the protein sequence of a gene, green if it falls within a gene but does not change the protein, and black if it does not fall within a gene. Tick marks are drawn at the top and bottom of each mutation's vertical bar to make the bar more visible when most alleles are reference alleles. Only single-nucleotide mutations are displayed, not insertions or deletions.

The phylogenetic tree showing inferred relationships between the samples is depicted in the left column of the display. Mousing over this will show the GISAID identifiers for the different samples. At the default track height, about 100 samples are averaged into each row of pixels. The track height can be adjusted in the track controls, which can be reached by clicking on the gray button to the left of the tree or by right-clicking on the image.


Rob Lanfear regularly runs the sarscov2phylo pipeline on all complete, high-coverage sequences available from GISAID. The pipeline aligns all sequences to the same reference genome used by the Genome Browser (RefSeq NC_045512.2, GenBank MN908947.3, GISAID sample hCoV-19/Wuhan/Hu-1/2019|EPI_ISL_402125|2019-12-31) using MAFFT (Katoh et al.). It masks sites identified as problematic by the ProblematicSites_SARS-CoV2 repository (De Maio et al., Turakhia et al.), as well as sites that are N's or gaps in >50% of samples. fasttree (Price et al.) is used to infer the phylogenetic tree; sequences on very long branches are removed using TreeShrink (Mai et al.). The tree is re-rooted to hCoV-19/Wuhan/WH04/2020|EPI_ISL_406801|2020-01-05.

For full details, see the sarscov2phylo documentation.

Collapsing of nodes that do not have an associated mutation is done using strain_phylogenetics (Turakhia et al.).

Data Access

You can download the VCF files underlying this track (gisaid.*.vcf.gz) from our Download Server. The data can be explored interactively with the Table Browser or the Data Integrator.

Note: while the VCF files contain mutations found in sequences collected by GISAID, they are not sufficient to reconstruct the original sequences available from GISAID due to treatment of ambiguous IUPAC bases as missing information in the VCF and omission of insertion and deletion mutations. Additionally, the subtracks that are filtered to include only mutations found in a minimum percentage of samples give very incomplete representations of samples. Researchers wishing to work with SARS-CoV-2 genomic sequences should register with GISAID and download the full sequences.


This work is made possible by the open sharing of genetic data by research groups from all over the world. We gratefully acknowledge their contributions. Sequences are collected by GISAID and may be downloaded by registered users.

Special thanks to Rob Lanfear for developing, running and sharing the sarscov2phylo pipeline and results.

Data usage policy

The data presented here is intended to rapidly disseminate analysis of important pathogens. Unpublished data is included with permission of the data generators, and does not impact their right to publish. Please contact the respective authors if you intend to carry out further research using their data. Author contact info is available via


Rambaut A, Holmes EC, O'Toole Á, Hill V, McCrone JT, Ruis C, du Plessis L, Pybus OG. A dynamic nomenclature proposal for SARS-CoV-2 lineages to assist genomic epidemiology. Nat Microbiol. 2020 Nov;5(11):1403-1407. PMID: 32669681

Alm E, Broberg EK, Connor T, Hodcroft EB, Komissarov AB, Maurer-Stroh S, Melidou A, Neher RA, O'Toole Á, Pereyaslov D et al. Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020. Euro Surveill. 2020 Aug;25(32). PMID: 32794443; PMC: PMC7427299

Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 2013 Apr;30(4):772-80. PMID: 23329690; PMC: PMC3603318

De Maio N, Walker C, Borges R, Weilguny L, Slodkowicz G, Goldman N. Masking strategies for SARS-CoV-2 alignments. 2020 May 13.

De Maio N, Gozashti L, Turakhia Y, Walker C, Lanfear R, Corbett-Detig R, Goldman N. Updated analysis with data from 12th June 2020. 2020 July 14.

Turakhia Y, Thornlow B, Gozashti L, Hinrichs AS, Fernandes JD, Haussler D, and Corbett-Detig R. Stability of SARS-CoV-2 Phylogenies. bioRxiv. 2020 June 9.

Price MN, Dehal PS, Arkin AP. FastTree 2--approximately maximum-likelihood trees for large alignments. PLoS One. 2010 Mar 10;5(3):e9490. PMID: 20224823; PMC: PMC2835736

Mai U, Mirarab S. TreeShrink: fast and accurate detection of outlier long branches in collections of phylogenetic trees. BMC Genomics. 2018 May 8;19(Suppl 5):272. PMID: 29745847; PMC: PMC5998883